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

rs56165452

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) CYP2C9*4 homozygote
(C;T) carrier of one CYP2C9*4 allele
(T;T) 0 normal
ReferenceGRCh38 38.1/142
Chromosome10
Position94981297
GeneCYP2C9
is asnp
is mentioned by
dbSNPrs56165452
ebirs56165452
HLIrs56165452
Exacrs56165452
Varsomers56165452
Maprs56165452
PheGenIrs56165452
hapmaprs56165452
1000 genomesrs56165452
hgdprs56165452
ensemblrs56165452
gopubmedrs56165452
geneviewrs56165452
scholarrs56165452
googlers56165452
pharmgkbrs56165452
gwascentralrs56165452
openSNPrs56165452
23andMers56165452
23andMe allrs56165452
SNP Nexus

SNPshotrs56165452
SNPdbers56165452
MSV3drs56165452
GWAS Ctlgrs56165452
Max Magnitude0
rs56165452, also known as 1076T>C, 42615T>C or I359T, is a SNP in the CYP2C9 gene.

The rs56165452(C) allele defines the CYP2C9*4 variant, which has decreased activity.

ClinVar
Risk rs56165452(A,C;A,C)
Alt rs56165452(A,C;A,C)
Reference rs56165452(T;T)
Significance Drug-response
Disease warfarin response - Dosage
Variation info
Gene CYP2C9
CLNDBN warfarin response - Dosage
Reversed 0
HGVS NC_000010.10:g.96741054T>A
CLNSRC PharmGKB Clinical Annotation PharmGKB
CLNACC RCV000211172.1,