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rs72558191

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs72558191(G;G)
Make rs72558191(G;T)
ReferenceGRCh38 38.1/141
Chromosome10
Position94947919
GeneCYP2C9
is asnp
is mentioned by
dbSNPrs72558191
ebirs72558191
HLIrs72558191
Exacrs72558191
Varsomers72558191
Maprs72558191
PheGenIrs72558191
hapmaprs72558191
1000 genomesrs72558191
hgdprs72558191
ensemblrs72558191
gopubmedrs72558191
geneviewrs72558191
scholarrs72558191
googlers72558191
pharmgkbrs72558191
gwascentralrs72558191
openSNPrs72558191
23andMers72558191
23andMe allrs72558191
SNP Nexus

SNPshotrs72558191
SNPdbers72558191
MSV3drs72558191
GWAS Ctlgrs72558191
Max Magnitude0
OMIM601130
Desc
Variant0003
Relatedalso


ClinVar
Risk rs72558191(G;G)
Alt rs72558191(G;G)
Reference rs72558191(T;T)
Significance Pathogenic
Disease Warfarin response
Variation info
Gene CYP2C9
CLNDBN Warfarin response
Reversed 0
HGVS NC_000010.10:g.96707676T>G
CLNSRC OMIM Allelic Variant
CLNACC RCV000008921.2,