rs12769205
From SNPedia
Orientation | plus |
Stabilized | plus |
Make rs12769205(A;A) |
Make rs12769205(A;G) |
Make rs12769205(G;G) |
Reference | GRCh38 38.1/142 |
Chromosome | 10 |
Position | 94775367 |
Gene | CYP2C19 |
is a | snp |
is | mentioned by |
dbSNP | rs12769205 |
dbSNP (classic) | rs12769205 |
ClinGen | rs12769205 |
ebi | rs12769205 |
HLI | rs12769205 |
Exac | rs12769205 |
Gnomad | rs12769205 |
Varsome | rs12769205 |
LitVar | rs12769205 |
Map | rs12769205 |
PheGenI | rs12769205 |
Biobank | rs12769205 |
1000 genomes | rs12769205 |
hgdp | rs12769205 |
ensembl | rs12769205 |
geneview | rs12769205 |
scholar | rs12769205 |
rs12769205 | |
pharmgkb | rs12769205 |
gwascentral | rs12769205 |
openSNP | rs12769205 |
23andMe | rs12769205 |
SNPshot | rs12769205 |
SNPdbe | rs12769205 |
MSV3d | rs12769205 |
GWAS Ctlg | rs12769205 |
Max Magnitude | 0 |
[PMID 26021325] The CYP2C19 Intron 2 Branch Point SNP is the Ancestral Polymorphism Contributing to the Poor Metabolizer Phenotype in Livers with CYP2C19*35 and CYP2C19*2 Alleles