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Select item 61541.

rs6154 [Homo sapiens]

Variant type:: SNV
Alleles:: G>A,C [Show Flanks]
Chromosome:: X:67643382 (GRCh38)
X:66863224 (GRCh37)
Canonical SPDI:: NC_000023.11:67643381:G:A,NC_000023.11:67643381:G:C
Gene:: AR (Varview)
Functional Consequence:: synonymous_variant,missense_variant,intron_variant,coding_sequence_variant
Clinical significance:: benign,likely-pathogenic
Validated:: by frequency,by alfa,by cluster
MAF:: A=0.0007833/81 (ALFA)
G=0./0 (SGDP_PRJ)
A=0.0003177/334 (GnomAD_exomes)
A=0.0012565/96 (ExAC)
A=0.0031169/342 (GnomAD_genomes)
A=0.0031217/15 (1000Genomes_30X)
A=0.0031241/33 (GoESP)
A=0.0031788/12 (1000Genomes)
A=0.0038045/1007 (TOPMED)
HGVS:: NC_000023.11:g.67643382G>A, NC_000023.11:g.67643382G>C, NC_000023.10:g.66863224G>A, NC_000023.10:g.66863224G>C, NG_009014.2:g.104351G>A, NG_009014.2:g.104351G>C, NM_000044.6:c.1743G>A, NM_000044.6:c.1743G>C, NM_000044.5:c.1743G>A, NM_000044.5:c.1743G>C, NM_000044.4:c.1743G>A, NM_000044.4:c.1743G>C, NM_000044.3:c.1743G>A, NM_000044.3:c.1743G>C, NM_001011645.3:c.147G>A, NM_001011645.3:c.147G>C, NM_001011645.2:c.147G>A, NM_001011645.2:c.147G>C, NM_001424175.1:c.1746G>A, NM_001424175.1:c.1746G>C, NM_001348061.1:c.1743G>A, NM_001348061.1:c.1743G>C, NM_001348063.1:c.1743G>A, NM_001348063.1:c.1743G>C, NP_000035.2:p.Lys581Asn, NP_001011645.1:p.Lys49Asn, NP_001334990.1:p.Lys581Asn, NP_001334992.1:p.Lys581Asn

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