rs72552799
From SNPedia
Orientation | plus |
Stabilized | plus |
Geno | Mag | Summary |
---|---|---|
(C;C) | 0 | normal |
(C;T) | carrier of one CYP3A4*8 allele | |
(T;T) | CYP3A4*8 homozygote |
Reference | GRCh38 38.1/141 |
Chromosome | 7 |
Position | 99770165 |
Gene | CYP3A4 |
is a | snp |
is | mentioned by |
dbSNP | rs72552799 |
dbSNP (classic) | rs72552799 |
ClinGen | rs72552799 |
ebi | rs72552799 |
HLI | rs72552799 |
Exac | rs72552799 |
Gnomad | rs72552799 |
Varsome | rs72552799 |
LitVar | rs72552799 |
Map | rs72552799 |
PheGenI | rs72552799 |
Biobank | rs72552799 |
1000 genomes | rs72552799 |
hgdp | rs72552799 |
ensembl | rs72552799 |
geneview | rs72552799 |
scholar | rs72552799 |
rs72552799 | |
pharmgkb | rs72552799 |
gwascentral | rs72552799 |
openSNP | rs72552799 |
23andMe | rs72552799 |
SNPshot | rs72552799 |
SNPdbe | rs72552799 |
MSV3d | rs72552799 |
GWAS Ctlg | rs72552799 |
Max Magnitude | 0 |
rs72552799, also known as 1389G>A, 13908G>A or R130Q, is a SNP in the CYP3A4 gene.
The rs72552799(T) allele defines the CYP3A4*8 variant.