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Select item 99344381.

rs9934438 [Homo sapiens]

Variant type:: SNV
Alleles:: G>A,C [Show Flanks]
Chromosome:: 16:31093557 (GRCh38)
16:31104878 (GRCh37)
Canonical SPDI:: NC_000016.10:31093556:G:A,NC_000016.10:31093556:G:C
Gene:: VKORC1 (Varview)
Functional Consequence:: intron_variant
Clinical significance:: drug-response,likely-benign,pathogenic,benign
Validated:: by frequency,by alfa,by cluster
MAF:: A=0.3812409/88791 (ALFA)
G=0.0754012/545 (Korea4K)
G=0.0785519/230 (KOREAN)
G=0.0933568/7226 (TOMMO)
A=0.1891386/101 (MGP)
G=0.1893204/39 (Vietnamese)
G=0.2601156/90 (SGDP_PRJ)
G=0.2727273/12 (Siberian)
A=0.3171813/47149 (GnomAD_genomes)
A=0.3227587/85431 (TOPMED)
A=0.3401688/26757 (PAGE_STUDY)
A=0.3438476/2202 (1000Genomes_30X)
A=0.3459821/1550 (Estonian)
A=0.3558307/1782 (1000Genomes)
A=0.3679294/1418 (ALSPAC)
A=0.3702805/1373 (TWINSUK)
A=0.3733333/224 (NorthernSweden)
A=0.378836/716 (HapMap)
A=0.3794491/506138 (GnomAD_exomes)
A=0.455595/513 (Daghestan)
A=0.4583333/99 (Qatari)
A=0.475/19 (GENOME_DK)
HGVS:: NC_000016.10:g.31093557G>A, NC_000016.10:g.31093557G>C, NC_000016.9:g.31104878G>A, NC_000016.9:g.31104878G>C, NG_011564.1:g.6399C>T, NG_011564.1:g.6399C>G, NG_139533.1:g.636G>A, NG_139533.1:g.636G>C

dbSNP