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Rs104894542

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Orientationminus
is asnp
is mentioned by
dbSNPrs104894542
PheGenIrs104894542
hapmaprs104894542
1000 genomesrs104894542
hgdprs104894542
ensemblrs104894542
gopubmedrs104894542
geneviewrs104894542
scholarrs104894542
googlers104894542
pharmgkbrs104894542
gwascentralrs104894542
openSNPrs104894542
23andMers104894542
23andMe allrs104894542
SNP Nexus

SNPshotrs104894542
SNPdbers104894542
MSV3drs104894542
GeneVKORC1
Merged fromRs28940305
Chromosome16
Orientationminus
Position31091243
ReferenceGRCh38 38.1/141
Max Magnitude0
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs104894542(G;G)
Make rs104894542(G;T)
OMIM608547
Desc
Variant0005
Relatedalso
ClinVar
Risk rs104894542(G;G)
Alt rs104894542(G;G)
Reference rs104894542(T;T)
Significance 5
Disease Warfarin response
ClinVar info
Gene VKORC1
CLNDBN Warfarin response
Reversed 1
CLNHGVS NC_000016.9:g.31102564A>C
CLNSRC OMIM Allelic Variant
CLNACC RCV000002294.1