Rs104894541

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Orientationminus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs104894541(A;G)
Make rs104894541(G;G)
ReferenceGRCh38 38.1/141
Chromosome16
Position31094558
GeneVKORC1
is asnp
is mentioned by
dbSNPrs104894541
Exacrs104894541
PheGenIrs104894541
nextbiors104894541
hapmaprs104894541
1000 genomesrs104894541
hgdprs104894541
ensemblrs104894541
gopubmedrs104894541
geneviewrs104894541
scholarrs104894541
googlers104894541
pharmgkbrs104894541
gwascentralrs104894541
openSNPrs104894541
23andMers104894541
23andMe allrs104894541
SNP Nexus

SNPshotrs104894541
SNPdbers104894541
MSV3drs104894541
Merged fromRs28940304
Max Magnitude0
OMIM608547
Desc
Variant0004
Relatedalso
ClinVar
Risk rs104894541(G;G)
Alt rs104894541(G;G)
Reference rs104894541(A;A)
Significance Pathogenic
Disease Warfarin response
Variation info
Gene VKORC1
CLNDBN Warfarin response
Reversed 1
HGVS NC_000016.9:g.31105879T>C
CLNSRC OMIM Allelic Variant
CLNACC RCV000002293.1,