rs2017319
From SNPedia
Orientation | plus |
Stabilized | plus |
Geno | Mag | Summary |
---|---|---|
(C;C) | 0 | normal |
(C;T) | carrier of one CYP2C9_50196C>T allele | |
(T;T) | CYP2C9_50196C>T homozygote |
Reference | GRCh38 38.1/142 |
Chromosome | 10 |
Position | 94988878 |
Gene | CYP2C9 |
is a | snp |
is | mentioned by |
dbSNP | rs2017319 |
dbSNP (classic) | rs2017319 |
ClinGen | rs2017319 |
ebi | rs2017319 |
HLI | rs2017319 |
Exac | rs2017319 |
Gnomad | rs2017319 |
Varsome | rs2017319 |
LitVar | rs2017319 |
Map | rs2017319 |
PheGenI | rs2017319 |
Biobank | rs2017319 |
1000 genomes | rs2017319 |
hgdp | rs2017319 |
ensembl | rs2017319 |
geneview | rs2017319 |
scholar | rs2017319 |
rs2017319 | |
pharmgkb | rs2017319 |
gwascentral | rs2017319 |
openSNP | rs2017319 |
23andMe | rs2017319 |
SNPshot | rs2017319 |
SNPdbe | rs2017319 |
MSV3d | rs2017319 |
GWAS Ctlg | rs2017319 |
GMAF | 0.02525 |
Max Magnitude | 0 |
? | (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 18698231] Polymorphisms affecting gene transcription and mRNA processing in pharmacogenetic candidate genes: detection through allelic expression imbalance in human target tissues.