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rs1057911

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(A;A) 0 normal
(A;T) 3 carrier of one CYP2C9_50298A>T allele
(T;T) 3 CYP2C9_50298A>T homozygote
ReferenceGRCh38 38.1/142
Chromosome10
Position94988980
GeneCYP2C9
is asnp
is mentioned by
dbSNPrs1057911
ebirs1057911
HLIrs1057911
Exacrs1057911
Varsomers1057911
Maprs1057911
PheGenIrs1057911
hapmaprs1057911
1000 genomesrs1057911
hgdprs1057911
ensemblrs1057911
gopubmedrs1057911
geneviewrs1057911
scholarrs1057911
googlers1057911
pharmgkbrs1057911
gwascentralrs1057911
openSNPrs1057911
23andMers1057911
23andMe allrs1057911
SNP Nexus

SNPshotrs1057911
SNPdbers1057911
MSV3drs1057911
GWAS Ctlgrs1057911
GMAF0.0427
Max Magnitude3
? (A;A) (A;T) (T;T) 28
rs1057911 is a SNP in the CYP2C9 gene.

The rs1057911(T) allele defines the CYP2C9_50298A>T variant, about which little is known.

Warfarin


[PMID 17048007OA-icon.png] Association of warfarin dose with genes involved in its action and metabolism.


[PMID 17368604] The association of CYP2C9 gene polymorphisms with colorectal carcinoma in Han Chinese.