rs72558185
From SNPedia
Orientation | plus |
Stabilized | plus |
Geno | Mag | Summary |
---|---|---|
(-;-) | 0 | normal |
(-;G) | carrier of one CYP2C19 hCV34328665 allele | |
(G;G) | CYP2C19 hCV34328665 homozygote |
Reference | GRCh38 38.1/142 |
Chromosome | 10 |
Position | 94781899 |
Gene | CYP2C19 |
is a | snp |
is | mentioned by |
dbSNP | rs72558185 |
dbSNP (classic) | rs72558185 |
ClinGen | rs72558185 |
ebi | rs72558185 |
HLI | rs72558185 |
Exac | rs72558185 |
Gnomad | rs72558185 |
Varsome | rs72558185 |
LitVar | rs72558185 |
Map | rs72558185 |
PheGenI | rs72558185 |
Biobank | rs72558185 |
1000 genomes | rs72558185 |
hgdp | rs72558185 |
ensembl | rs72558185 |
geneview | rs72558185 |
scholar | rs72558185 |
rs72558185 | |
pharmgkb | rs72558185 |
gwascentral | rs72558185 |
openSNP | rs72558185 |
23andMe | rs72558185 |
SNPshot | rs72558185 |
SNPdbe | rs72558185 |
MSV3d | rs72558185 |
GWAS Ctlg | rs72558185 |
Max Magnitude | 0 |
The rs72558185(G) SNP is an insertion variant in the CYP2C19 gene; it is also known as hCV34328665, and is in the Affymetrix DMET panel.