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rs104894539

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs104894539(G;T)
Make rs104894539(T;T)
ReferenceGRCh38 38.1/141
Chromosome16
Position31094645
GeneVKORC1
is asnp
is mentioned by
dbSNPrs104894539
ebirs104894539
HLIrs104894539
Exacrs104894539
Varsomers104894539
Maprs104894539
PheGenIrs104894539
hapmaprs104894539
1000 genomesrs104894539
hgdprs104894539
ensemblrs104894539
gopubmedrs104894539
geneviewrs104894539
scholarrs104894539
googlers104894539
pharmgkbrs104894539
gwascentralrs104894539
openSNPrs104894539
23andMers104894539
23andMe allrs104894539
SNP Nexus

SNPshotrs104894539
SNPdbers104894539
MSV3drs104894539
GWAS Ctlgrs104894539
Max Magnitude0
OMIM608547
Desc
Variant0002
Relatedalso
ClinVar
Risk rs104894539(T;T)
Alt rs104894539(T;T)
Reference rs104894539(G;G)
Significance Pathogenic
Disease Warfarin response
Variation info
Gene VKORC1
CLNDBN Warfarin response
Reversed 1
HGVS NC_000016.9:g.31105966C>A
CLNSRC OMIM Allelic Variant
CLNACC RCV000002291.2,