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rs2017319

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 normal
(C;T) carrier of one CYP2C9_50196C>T allele
(T;T) CYP2C9_50196C>T homozygote
ReferenceGRCh38 38.1/142
Chromosome10
Position94988878
GeneCYP2C9
is asnp
is mentioned by
dbSNPrs2017319
dbSNP (classic)rs2017319
ClinGenrs2017319
ebirs2017319
HLIrs2017319
Exacrs2017319
Gnomadrs2017319
Varsomers2017319
LitVarrs2017319
Maprs2017319
PheGenIrs2017319
Biobankrs2017319
1000 genomesrs2017319
hgdprs2017319
ensemblrs2017319
geneviewrs2017319
scholarrs2017319
googlers2017319
pharmgkbrs2017319
gwascentralrs2017319
openSNPrs2017319
23andMers2017319
SNPshotrs2017319
SNPdbers2017319
MSV3drs2017319
GWAS Ctlgrs2017319
GMAF0.02525
Max Magnitude0
? (C;C) (C;T) (T;T) 28


rs2017319 is a SNP in the CYP2C9 gene.

The rs2017319(T) allele defines the CYP2C9_50196C>T variant, about which little is known.

[PMID 18698231OA-icon.png] Polymorphisms affecting gene transcription and mRNA processing in pharmacogenetic candidate genes: detection through allelic expression imbalance in human target tissues.