Have questions? Visit https://www.reddit.com/r/SNPedia

rs397509427

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(;) 0 common in clinvar
Make rs397509427(-;-)
Make rs397509427(-;G)
Make rs397509427(G;G)
ReferenceGRCh38 38.1/141
Chromosome16
Position31096316
GeneVKORC1
is asnp
is mentioned by
dbSNPrs397509427
ebirs397509427
HLIrs397509427
Exacrs397509427
Varsomers397509427
Maprs397509427
PheGenIrs397509427
hapmaprs397509427
1000 genomesrs397509427
hgdprs397509427
ensemblrs397509427
gopubmedrs397509427
geneviewrs397509427
scholarrs397509427
googlers397509427
pharmgkbrs397509427
gwascentralrs397509427
openSNPrs397509427
23andMers397509427
23andMe allrs397509427
SNP Nexus

SNPshotrs397509427
SNPdbers397509427
MSV3drs397509427
GWAS Ctlgrs397509427
Max Magnitude0
ClinVar
Risk rs397509427(G;G)
Alt rs397509427(G;G)
Reference rs397509427(;)
Significance Drug-response
Disease Warfarin response
Variation info
Gene VKORC1
CLNDBN Warfarin response
Reversed 1
HGVS NC_000016.9:g.31107638dupC
CLNSRC ClinVar
CLNACC RCV000054486.1,