rs72558190
From SNPedia
Orientation | plus |
Stabilized | plus |
Geno | Mag | Summary |
---|---|---|
(A;A) | CYP2C9*15 homozygote | |
(A;C) | carrier of one CYP2C9*15 allele | |
(C;C) | 0 | normal |
Reference | GRCh38 38.1/142 |
Chromosome | 10 |
Position | 94947782 |
Gene | CYP2C9 |
is a | snp |
is | mentioned by |
dbSNP | rs72558190 |
dbSNP (classic) | rs72558190 |
ClinGen | rs72558190 |
ebi | rs72558190 |
HLI | rs72558190 |
Exac | rs72558190 |
Gnomad | rs72558190 |
Varsome | rs72558190 |
LitVar | rs72558190 |
Map | rs72558190 |
PheGenI | rs72558190 |
Biobank | rs72558190 |
1000 genomes | rs72558190 |
hgdp | rs72558190 |
ensembl | rs72558190 |
geneview | rs72558190 |
scholar | rs72558190 |
rs72558190 | |
pharmgkb | rs72558190 |
gwascentral | rs72558190 |
openSNP | rs72558190 |
23andMe | rs72558190 |
SNPshot | rs72558190 |
SNPdbe | rs72558190 |
MSV3d | rs72558190 |
GWAS Ctlg | rs72558190 |
Max Magnitude | 0 |
rs72558190, also known as 485C>A or S162X, is a SNP in the CYP2C9 gene.
The rs72558190(A) allele defines the CYP2C9*15 variant, which is inactive.