dbSNP Short Genetic Variations
Welcome to the Reference SNP (rs) Report
All alleles are reported in the Forward orientation. Click on the Variant Details tab for details on Genomic Placement, Gene, and Amino Acid changes. HGVS names are in the HGVS tab.
Reference SNP (rs) Report
This page reports data for a single dbSNP Reference SNP variation (RefSNP or rs) from the new redesigned dbSNP build.
Top of the page reports a concise summary for the rs, with more specific details included in the corresponding tabs below.
All alleles are reported in the Forward orientation. Use the Genomic View to inspect the nucleotides flanking the variant, and its neighbors.
For more information see Help documentation.
rs6445
Current Build 156
Released September 21, 2022
- Organism
- Homo sapiens
- Position
-
chr6:32041006 (GRCh38.p14) Help
The anchor position for this RefSNP. Includes all nucleotides potentially affected by this change, thus it can differ from HGVS, which is right-shifted. See here for details.
- Alleles
- C>T
- Variation Type
- SNV Single Nucleotide Variation
- Frequency
-
T=0.005304 (741/139700, GnomAD)T=0.004597 (633/137706, GnomAD_exome)T=0.00466 (118/25318, ALFA) (+ 5 more)
- Clinical Significance
- Reported in ClinVar
- Gene : Consequence
-
CYP21A2 : Missense VariantTNXB : 500B Downstream Variant
- Publications
- 5 citations
- Genomic View
- See rs on genome
ALFA Allele Frequency
The ALFA project provide aggregate allele frequency from dbGaP. More information is available on the project page including descriptions, data access, and terms of use.
| Population | Group | Sample Size | Ref Allele | Alt Allele | Ref HMOZ | Alt HMOZ | HTRZ | HWEP |
|---|---|---|---|---|---|---|---|---|
| Total | Global | 25318 | C=0.99534 | T=0.00466 | 0.990679 | 0.0 | 0.009321 | 0 |
| European | Sub | 18140 | C=0.99471 | T=0.00529 | 0.989416 | 0.0 | 0.010584 | 0 |
| African | Sub | 3410 | C=0.9988 | T=0.0012 | 0.997654 | 0.0 | 0.002346 | 0 |
| African Others | Sub | 116 | C=1.000 | T=0.000 | 1.0 | 0.0 | 0.0 | N/A |
| African American | Sub | 3294 | C=0.9988 | T=0.0012 | 0.997571 | 0.0 | 0.002429 | 0 |
| Asian | Sub | 164 | C=1.000 | T=0.000 | 1.0 | 0.0 | 0.0 | N/A |
| East Asian | Sub | 110 | C=1.000 | T=0.000 | 1.0 | 0.0 | 0.0 | N/A |
| Other Asian | Sub | 54 | C=1.00 | T=0.00 | 1.0 | 0.0 | 0.0 | N/A |
| Latin American 1 | Sub | 146 | C=1.000 | T=0.000 | 1.0 | 0.0 | 0.0 | N/A |
| Latin American 2 | Sub | 610 | C=0.997 | T=0.003 | 0.993443 | 0.0 | 0.006557 | 0 |
| South Asian | Sub | 94 | C=1.00 | T=0.00 | 1.0 | 0.0 | 0.0 | N/A |
| Other | Sub | 2754 | C=0.9942 | T=0.0058 | 0.988381 | 0.0 | 0.011619 | 0 |
Frequency tab displays a table of the reference and alternate allele frequencies reported by various studies and populations. Table lines, where Population="Global" refer to the entire study population, whereas lines, where Group="Sub", refer to a study-specific population subgroupings (i.e. AFR, CAU, etc.), if available. Frequency for the alternate allele (Alt Allele) is a ratio of samples observed-to-total, where the numerator (observed samples) is the number of chromosomes in the study with the minor allele present (found in "Sample size", where Group="Sub"), and the denominator (total samples) is the total number of all chromosomes in the study for the variant (found in "Sample size", where Group="Study-wide" and Population="Global").
Download| Study | Population | Group | Sample Size | Ref Allele | Alt Allele |
|---|---|---|---|---|---|
| gnomAD - Genomes | Global | Study-wide | 139700 | C=0.994696 | T=0.005304 |
| gnomAD - Genomes | European | Sub | 75480 | C=0.99189 | T=0.00811 |
| gnomAD - Genomes | African | Sub | 42012 | C=0.99819 | T=0.00181 |
| gnomAD - Genomes | American | Sub | 13632 | C=0.99685 | T=0.00315 |
| gnomAD - Genomes | Ashkenazi Jewish | Sub | 3316 | C=0.9991 | T=0.0009 |
| gnomAD - Genomes | East Asian | Sub | 3128 | C=1.0000 | T=0.0000 |
| gnomAD - Genomes | Other | Sub | 2132 | C=0.9967 | T=0.0033 |
| gnomAD - Exomes | Global | Study-wide | 137706 | C=0.995403 | T=0.004597 |
| gnomAD - Exomes | European | Sub | 60082 | C=0.99153 | T=0.00847 |
| gnomAD - Exomes | Asian | Sub | 33586 | C=0.99946 | T=0.00054 |
| gnomAD - Exomes | American | Sub | 24654 | C=0.99680 | T=0.00320 |
| gnomAD - Exomes | Ashkenazi Jewish | Sub | 8228 | C=0.9996 | T=0.0004 |
| gnomAD - Exomes | African | Sub | 7012 | C=0.9989 | T=0.0011 |
| gnomAD - Exomes | Other | Sub | 4144 | C=0.9961 | T=0.0039 |
| Allele Frequency Aggregator | Total | Global | 25318 | C=0.99534 | T=0.00466 |
| Allele Frequency Aggregator | European | Sub | 18140 | C=0.99471 | T=0.00529 |
| Allele Frequency Aggregator | African | Sub | 3410 | C=0.9988 | T=0.0012 |
| Allele Frequency Aggregator | Other | Sub | 2754 | C=0.9942 | T=0.0058 |
| Allele Frequency Aggregator | Latin American 2 | Sub | 610 | C=0.997 | T=0.003 |
| Allele Frequency Aggregator | Asian | Sub | 164 | C=1.000 | T=0.000 |
| Allele Frequency Aggregator | Latin American 1 | Sub | 146 | C=1.000 | T=0.000 |
| Allele Frequency Aggregator | South Asian | Sub | 94 | C=1.00 | T=0.00 |
| ExAC | Global | Study-wide | 12730 | C=0.99772 | T=0.00228 |
| ExAC | Asian | Sub | 7996 | C=0.9994 | T=0.0006 |
| ExAC | Europe | Sub | 3586 | C=0.9941 | T=0.0059 |
| ExAC | African | Sub | 792 | C=1.000 | T=0.000 |
| ExAC | American | Sub | 226 | C=0.991 | T=0.009 |
| ExAC | Other | Sub | 130 | C=0.992 | T=0.008 |
| 1000Genomes_30x | Global | Study-wide | 6404 | C=0.9983 | T=0.0017 |
| 1000Genomes_30x | African | Sub | 1786 | C=0.9994 | T=0.0006 |
| 1000Genomes_30x | Europe | Sub | 1266 | C=0.9937 | T=0.0063 |
| 1000Genomes_30x | South Asian | Sub | 1202 | C=1.0000 | T=0.0000 |
| 1000Genomes_30x | East Asian | Sub | 1170 | C=1.0000 | T=0.0000 |
| 1000Genomes_30x | American | Sub | 980 | C=0.998 | T=0.002 |
| 1000Genomes | Global | Study-wide | 5008 | C=0.9982 | T=0.0018 |
| 1000Genomes | African | Sub | 1322 | C=0.9992 | T=0.0008 |
| 1000Genomes | East Asian | Sub | 1008 | C=1.0000 | T=0.0000 |
| 1000Genomes | Europe | Sub | 1006 | C=0.9940 | T=0.0060 |
| 1000Genomes | South Asian | Sub | 978 | C=1.000 | T=0.000 |
| 1000Genomes | American | Sub | 694 | C=0.997 | T=0.003 |
| The Danish reference pan genome | Danish | Study-wide | 40 | C=0.97 | T=0.03 |
| SGDP_PRJ | Global | Study-wide | 4 | C=0.2 | T=0.8 |
Variant Details tab shows known variant placements on genomic sequences: chromosomes (NC_), RefSeqGene, pseudogenes or genomic regions (NG_), and in a separate table: on transcripts (NM_) and protein sequences (NP_). The corresponding transcript and protein locations are listed in adjacent lines, along with molecular consequences from Sequence Ontology. When no protein placement is available, only the transcript is listed. Column "Codon[Amino acid]" shows the actual base change in the format of "Reference > Alternate" allele, including the nucleotide codon change in transcripts, and the amino acid change in proteins, respectively, allowing for known ribosomal slippage sites. To view nucleotides adjacent to the variant use the Genomic View at the bottom of the page - zoom into the sequence until the nucleotides around the variant become visible.
| Sequence name | Change |
|---|---|
| GRCh38.p14 chr 6 | NC_000006.12:g.32041006C>T |
| GRCh37.p13 chr 6 | NC_000006.11:g.32008783C>T |
| CYP21A2 RefSeqGene (LRG_829) | NG_007941.3:g.7702C>T |
| TNXB RefSeqGene | NG_008337.2:g.73369G>A |
| GRCh38.p14 chr 6 alt locus HSCHR6_MHC_COX_CTG1 | NT_113891.3:g.3479328C>T |
| GRCh37.p13 chr 6 alt locus HSCHR6_MHC_COX_CTG1 | NT_113891.2:g.3479434C>T |
| LOC106780800 genomic region | NG_045215.1:g.3235C>T |
| GRCh38.p14 chr 6 alt locus HSCHR6_MHC_DBB_CTG1 | NT_167245.2:g.3282414C>T |
| GRCh37.p13 chr 6 alt locus HSCHR6_MHC_DBB_CTG1 | NT_167245.1:g.3287999C>T |
| GRCh38.p14 chr 6 alt locus HSCHR6_MHC_SSTO_CTG1 | NT_167249.2:g.3342193C>T |
| GRCh37.p13 chr 6 alt locus HSCHR6_MHC_SSTO_CTG1 | NT_167249.1:g.3341491C>T |
| GRCh38.p14 chr 6 alt locus HSCHR6_MHC_MCF_CTG1 | NT_167247.2:g.3383039C>T |
| GRCh37.p13 chr 6 alt locus HSCHR6_MHC_MCF_CTG1 | NT_167247.1:g.3388624C>T |
| Molecule type | Change | Amino acid[Codon] | SO Term |
|---|---|---|---|
| TNXB transcript variant 3 | NM_001365276.2:c. | N/A | Downstream Transcript Variant |
| TNXB transcript variant XB | NM_019105.8:c. | N/A | Downstream Transcript Variant |
| TNXB transcript variant XB-S | NM_032470.4:c. | N/A | Downstream Transcript Variant |
| Molecule type | Change | Amino acid[Codon] | SO Term |
|---|---|---|---|
| CYP21A2 transcript variant 1 | NM_000500.9:c.1360C>T | P [CCC] > S [TCC] | Coding Sequence Variant |
| steroid 21-hydroxylase isoform a | NP_000491.4:p.Pro454Ser | P (Pro) > S (Ser) | Missense Variant |
| CYP21A2 transcript variant 4 | NM_001368144.2:c.955C>T | P [CCC] > S [TCC] | Coding Sequence Variant |
| steroid 21-hydroxylase isoform c | NP_001355073.1:p.Pro319Ser | P (Pro) > S (Ser) | Missense Variant |
| CYP21A2 transcript variant 2 | NM_001128590.4:c.1270C>T | P [CCC] > S [TCC] | Coding Sequence Variant |
| steroid 21-hydroxylase isoform b | NP_001122062.3:p.Pro424Ser | P (Pro) > S (Ser) | Missense Variant |
| CYP21A2 transcript variant 3 | NM_001368143.2:c.955C>T | P [CCC] > S [TCC] | Coding Sequence Variant |
| steroid 21-hydroxylase isoform c | NP_001355072.1:p.Pro319Ser | P (Pro) > S (Ser) | Missense Variant |
Clinical Significance tab shows a list of clinical significance entries from ClinVar associated with the variation, per allele. Click on the RCV accession (i.e. RCV000001615.2) or Allele ID (i.e. 12274) to access full ClinVar report.
| ClinVar Accession | Disease Names | Clinical Significance |
|---|---|---|
| RCV000012942.2 | Classic congenital adrenal hyperplasia due to 21-hydroxylase deficiency | Pathogenic |
| RCV000012943.11 | Classic congenital adrenal hyperplasia due to 21-hydroxylase deficiency | Pathogenic |
| RCV000012952.2 | Classic congenital adrenal hyperplasia due to 21-hydroxylase deficiency | Pathogenic |
| RCV000711371.16 | not provided | Pathogenic |
Aliases tab displays HGVS names representing the variant placements and allele changes on genomic, transcript and protein sequences, per allele. HGVS name is an expression for reporting sequence accession and version, sequence type, position, and allele change. The column "Note" can have two values: "diff" means that there is a difference between the reference allele (variation interval) at the placement reported in HGVS name and the reference alleles reported in other HGVS names, and "rev" means that the sequence of this variation interval at the placement reported in HGVS name is in reverse orientation to the sequence(s) of this variation in other HGVS names not labeled as "rev".
| Placement | C= | T |
|---|---|---|
| GRCh38.p14 chr 6 | NC_000006.12:g.32041006= | NC_000006.12:g.32041006C>T |
| GRCh37.p13 chr 6 | NC_000006.11:g.32008783= | NC_000006.11:g.32008783C>T |
| CYP21A2 RefSeqGene (LRG_829) | NG_007941.3:g.7702= | NG_007941.3:g.7702C>T |
| CYP21A2 transcript variant 1 | NM_000500.9:c.1360= | NM_000500.9:c.1360C>T |
| CYP21A2 transcript variant 1 | NM_000500.8:c.1360= | NM_000500.8:c.1360C>T |
| CYP21A2 transcript variant 1 | NM_000500.7:c.1360= | NM_000500.7:c.1360C>T |
| CYP21A2 transcript variant 2 | NM_001128590.4:c.1270= | NM_001128590.4:c.1270C>T |
| CYP21A2 transcript variant 2 | NM_001128590.3:c.1270= | NM_001128590.3:c.1270C>T |
| CYP21A2 transcript variant 3 | NM_001368143.2:c.955= | NM_001368143.2:c.955C>T |
| CYP21A2 transcript variant 3 | NM_001368143.1:c.955= | NM_001368143.1:c.955C>T |
| CYP21A2 transcript variant 4 | NM_001368144.2:c.955= | NM_001368144.2:c.955C>T |
| CYP21A2 transcript variant 4 | NM_001368144.1:c.955= | NM_001368144.1:c.955C>T |
| TNXB RefSeqGene | NG_008337.2:g.73369= | NG_008337.2:g.73369G>A |
| GRCh38.p14 chr 6 alt locus HSCHR6_MHC_COX_CTG1 | NT_113891.3:g.3479328= | NT_113891.3:g.3479328C>T |
| GRCh37.p13 chr 6 alt locus HSCHR6_MHC_COX_CTG1 | NT_113891.2:g.3479434= | NT_113891.2:g.3479434C>T |
| LOC106780800 genomic region | NG_045215.1:g.3235= | NG_045215.1:g.3235C>T |
| GRCh38.p14 chr 6 alt locus HSCHR6_MHC_DBB_CTG1 | NT_167245.2:g.3282414= | NT_167245.2:g.3282414C>T |
| GRCh37.p13 chr 6 alt locus HSCHR6_MHC_DBB_CTG1 | NT_167245.1:g.3287999= | NT_167245.1:g.3287999C>T |
| GRCh38.p14 chr 6 alt locus HSCHR6_MHC_SSTO_CTG1 | NT_167249.2:g.3342193= | NT_167249.2:g.3342193C>T |
| GRCh37.p13 chr 6 alt locus HSCHR6_MHC_SSTO_CTG1 | NT_167249.1:g.3341491= | NT_167249.1:g.3341491C>T |
| GRCh38.p14 chr 6 alt locus HSCHR6_MHC_MCF_CTG1 | NT_167247.2:g.3383039= | NT_167247.2:g.3383039C>T |
| GRCh37.p13 chr 6 alt locus HSCHR6_MHC_MCF_CTG1 | NT_167247.1:g.3388624= | NT_167247.1:g.3388624C>T |
| steroid 21-hydroxylase isoform a | NP_000491.4:p.Pro454= | NP_000491.4:p.Pro454Ser |
| steroid 21-hydroxylase isoform b | NP_001122062.3:p.Pro424= | NP_001122062.3:p.Pro424Ser |
| steroid 21-hydroxylase isoform c | NP_001355072.1:p.Pro319= | NP_001355072.1:p.Pro319Ser |
| steroid 21-hydroxylase isoform c | NP_001355073.1:p.Pro319= | NP_001355073.1:p.Pro319Ser |
Submissions tab displays variations originally submitted to dbSNP, now supporting this RefSNP cluster (rs). We display Submitter handle, Submission identifier, Date and Build number, when the submission appeared for the first time. Direct submissions to dbSNP have Submission ID in the form of an ss-prefixed number (ss#). Other supporting variations are listed in the table without ss#.
| No | Submitter | Submission ID | Date (Build) |
|---|---|---|---|
| 1 | WIAF-CSNP | ss8096 | Sep 19, 2000 (52) |
| 2 | OMIM-CURATED-RECORDS | ss288288403 | Dec 21, 2010 (133) |
| 3 | 1000GENOMES | ss1319569228 | Aug 21, 2014 (142) |
| 4 | EVA_GENOME_DK | ss1581608002 | Apr 01, 2015 (144) |
| 5 | EVA_EXAC | ss1688248356 | Apr 01, 2015 (144) |
| 6 | GNOMAD | ss2735676940 | Nov 08, 2017 (151) |
| 7 | GNOMAD | ss2747589692 | Nov 08, 2017 (151) |
| 8 | GNOMAD | ss2837460705 | Nov 08, 2017 (151) |
| 9 | SWEGEN | ss2998801788 | Nov 08, 2017 (151) |
| 10 | EVA | ss3825694990 | Apr 26, 2020 (154) |
| 11 | SGDP_PRJ | ss3864261331 | Apr 26, 2020 (154) |
| 12 | EVA | ss5237645973 | Oct 17, 2022 (156) |
| 13 | 1000G_HIGH_COVERAGE | ss5267946972 | Oct 17, 2022 (156) |
| 14 | EVA | ss5364740991 | Oct 17, 2022 (156) |
| 15 | 1000G_HIGH_COVERAGE | ss5553607631 | Oct 17, 2022 (156) |
| 16 | SANFORD_IMAGENETICS | ss5640095321 | Oct 17, 2022 (156) |
| 17 | EVA | ss5979780734 | Oct 17, 2022 (156) |
| 18 | 1000Genomes | NC_000006.11 - 32008783 | Oct 12, 2018 (152) |
| 19 | 1000Genomes_30x | NC_000006.12 - 32041006 | Oct 17, 2022 (156) |
| 20 | ExAC | NC_000006.11 - 32008783 | Oct 12, 2018 (152) |
| 21 | The Danish reference pan genome | NC_000006.11 - 32008783 | Apr 26, 2020 (154) |
| 22 | gnomAD - Genomes | NC_000006.12 - 32041006 | Apr 26, 2021 (155) |
| 23 | gnomAD - Exomes | NC_000006.11 - 32008783 | Jul 13, 2019 (153) |
| 24 | SGDP_PRJ | NC_000006.11 - 32008783 | Apr 26, 2020 (154) |
| 25 | ALFA | NC_000006.12 - 32041006 | Apr 26, 2021 (155) |
| 26 | ClinVar | RCV000012942.2 | Oct 17, 2022 (156) |
| 27 | ClinVar | RCV000012943.11 | Oct 17, 2022 (156) |
| 28 | ClinVar | RCV000012952.2 | Oct 17, 2022 (156) |
| 29 | ClinVar | RCV000711371.16 | Oct 17, 2022 (156) |
History tab displays RefSNPs (Associated ID) from previous builds (Build) that now support the current RefSNP, and the dates, when the history was updated for each Associated ID (History Updated).
| Submission IDs | Observation SPDI | Canonical SPDI | Source RSIDs |
|---|---|---|---|
| 31337092, 8274910, 7772941, 4819458, 16278311, ss1319569228, ss1581608002, ss1688248356, ss2735676940, ss2747589692, ss2837460705, ss2998801788, ss3825694990, ss3864261331, ss5364740991, ss5640095321, ss5979780734 | NC_000006.11:32008782:C:T | NC_000006.12:32041005:C:T | (self) |
| RCV000012942.2, RCV000012943.11, RCV000012952.2, RCV000711371.16, 41133566, 221301898, 2614803913, ss288288403, ss5237645973, ss5267946972, ss5553607631 | NC_000006.12:32041005:C:T | NC_000006.12:32041005:C:T | (self) |
| ss8096 | NT_007592.15:31948782:C:T | NC_000006.12:32041005:C:T | (self) |
Publications tab displays PubMed articles citing the variation as a listing of PMID, Title, Author, Year, Journal, ordered by Year, descending.
| PMID | Title | Author | Year | Journal |
|---|---|---|---|---|
| 1406699 | Pro-453 to Ser mutation in CYP21 is associated with nonclassic steroid 21-hydroxylase deficiency. | Owerbach D et al. | 1992 | Molecular endocrinology (Baltimore, Md.) |
| 10720040 | Predicting phenotype in steroid 21-hydroxylase deficiency? Comprehensive genotyping in 155 unrelated, well defined patients from southern Germany. | Krone N et al. | 2000 | The Journal of clinical endocrinology and metabolism |
| 18381579 | Inhibition of CYP21A2 enzyme activity caused by novel missense mutations identified in Brazilian and Scandinavian patients. | Soardi FC et al. | 2008 | The Journal of clinical endocrinology and metabolism |
| 20301350 | 21-Hydroxylase-Deficient Congenital Adrenal Hyperplasia. | Nimkarn S et al. | 1993 | GeneReviews(®) |
| 25741868 | Standards and guidelines for the interpretation of sequence variants: a joint consensus recommendation of the American College of Medical Genetics and Genomics and the Association for Molecular Pathology. | Richards S et al. | 2015 | Genetics in medicine |
The Flanks tab provides retrieving flanking sequences of a SNP on all molecules that have placements.
Genomic regions, transcripts, and products
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Help
NCBI Graphical Sequence Viewer display of the genomic region, transcripts and protein products for the reported RefSNP (rs).
Use the zoom option to view the nucleotides around the RefSNP and find other neighboring RefSNPs.
Visit Sequence Viewer for help with navigating inside the display and modifying the selection of displayed data tracks.
NCBI Graphical Sequence Viewer display of the genomic region, transcripts and protein products for the reported RefSNP (rs).
Use the zoom option to view the nucleotides around the RefSNP and find other neighboring RefSNPs.
Visit Sequence Viewer for help with navigating inside the display and modifying the selection of displayed data tracks.