Rs104894540

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Orientationminus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs104894540(C;C)
Make rs104894540(C;T)
ReferenceGRCh38 38.1/141
Chromosome16
Position31094596
GeneVKORC1
is asnp
is mentioned by
dbSNPrs104894540
PheGenIrs104894540
nextbiors104894540
hapmaprs104894540
1000 genomesrs104894540
hgdprs104894540
ensemblrs104894540
gopubmedrs104894540
geneviewrs104894540
scholarrs104894540
googlers104894540
pharmgkbrs104894540
gwascentralrs104894540
openSNPrs104894540
23andMers104894540
23andMe allrs104894540
SNP Nexus

SNPshotrs104894540
SNPdbers104894540
MSV3drs104894540
Merged fromRs28940303
Max Magnitude0
OMIM608547
Desc
Variant0003
Relatedalso
ClinVar
Risk rs104894540(C;C)
Alt rs104894540(C;C)
Reference rs104894540(T;T)
Significance Pathogenic
Disease Warfarin response
Variation info
Gene VKORC1
CLNDBN Warfarin response
Reversed 1
HGVS NC_000016.9:g.31105917A>G
CLNSRC OMIM Allelic Variant
CLNACC RCV000002292.1,