rs56165452

Orientation

plus

Stabilized

plus

Geno	Mag	Summary
(C;C)		CYP2C9*4 homozygote
(C;T)		carrier of one CYP2C9*4 allele
(T;T)	0	normal

Reference

GRCh38 38.1/142

Chromosome

10

Position

94981297

Gene

CYP2C9

is a	snp
is	mentioned by
dbSNP	rs56165452
dbSNP (classic)	rs56165452
ClinGen	rs56165452
ebi	rs56165452
HLI	rs56165452
Exac	rs56165452
Gnomad	rs56165452
Varsome	rs56165452
LitVar	rs56165452
Map	rs56165452
PheGenI	rs56165452
Biobank	rs56165452
1000 genomes	rs56165452
hgdp	rs56165452
ensembl	rs56165452
geneview	rs56165452
scholar	rs56165452
google	rs56165452
pharmgkb	rs56165452
gwascentral	rs56165452
openSNP	rs56165452
23andMe	rs56165452
SNPshot	rs56165452
SNPdbe	rs56165452
MSV3d	rs56165452
GWAS Ctlg	rs56165452

Max Magnitude

0

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;A) Rs56165452(C;C)
Alt	rs56165452(A;A) Rs56165452(C;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>C
CLNSRC	PharmGKB Clinical Annotation PharmGKB
CLNACC	RCV000417168.1,