Rs104894542

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Orientationminus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs104894542(G;G)
Make rs104894542(G;T)
ReferenceGRCh38 38.1/141
Chromosome16
Position31091243
GeneVKORC1
is asnp
is mentioned by
dbSNPrs104894542
PheGenIrs104894542
nextbiors104894542
hapmaprs104894542
1000 genomesrs104894542
hgdprs104894542
ensemblrs104894542
gopubmedrs104894542
geneviewrs104894542
scholarrs104894542
googlers104894542
pharmgkbrs104894542
gwascentralrs104894542
openSNPrs104894542
23andMers104894542
23andMe allrs104894542
SNP Nexus

SNPshotrs104894542
SNPdbers104894542
MSV3drs104894542
Merged fromRs28940305
Max Magnitude0
OMIM608547
Desc
Variant0005
Relatedalso
ClinVar
Risk rs104894542(G;G)
Alt rs104894542(G;G)
Reference rs104894542(T;T)
Significance Pathogenic
Disease Warfarin response
Variation info
Gene VKORC1
CLNDBN Warfarin response
Reversed 1
HGVS NC_000016.9:g.31102564A>C
CLNSRC OMIM Allelic Variant
CLNACC RCV000002294.1,