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rs7196161

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(A;A) 0 common genotype
(G;G) 0 common in clinvar
Make rs7196161(A;G)
ReferenceGRCh38 38.1/141
Chromosome16
Position31099660
is asnp
is mentioned by
dbSNPrs7196161
dbSNP (classic)rs7196161
ClinGenrs7196161
ebirs7196161
HLIrs7196161
Exacrs7196161
Gnomadrs7196161
Varsomers7196161
LitVarrs7196161
Maprs7196161
PheGenIrs7196161
Biobankrs7196161
1000 genomesrs7196161
hgdprs7196161
ensemblrs7196161
geneviewrs7196161
scholarrs7196161
googlers7196161
pharmgkbrs7196161
gwascentralrs7196161
openSNPrs7196161
23andMers7196161
SNPshotrs7196161
SNPdbers7196161
MSV3drs7196161
GWAS Ctlgrs7196161
GMAF0.4458
Max Magnitude0

[PMID 23662025OA-icon.png] Genetic variation and haplotype structure of the gene Vitamin K epoxide reductase complex, subunit 1 in the Tamilian population


[PMID 18523153OA-icon.png] Regulatory polymorphism in vitamin K epoxide reductase complex subunit 1 (VKORC1) affects gene expression and warfarin dose requirement.


[PMID 18752379OA-icon.png] Warfarin pharmacogenetics.


[PMID 18855533OA-icon.png] VKORC1 polymorphisms, haplotypes and haplotype groups on warfarin dose among African-Americans and European-Americans.


ClinVar
Risk Rs7196161(A;A)
Alt Rs7196161(A;A)
Reference Rs7196161(G;G)
Significance Drug-response
Disease warfarin response - Dosage
Variation info
Gene
CLNDBN warfarin response - Dosage
Reversed 0
HGVS NC_000016.9:g.31110981G>A
CLNSRC PharmGKB Clinical Annotation
CLNACC RCV000211249.1,