rs41279854
From SNPedia
Orientation | plus |
Stabilized | plus |
Geno | Mag | Summary |
---|---|---|
(A;A) | 0 | normal |
(A;G) | 2 | carrier of one CYP3A5*10 allele |
(G;G) | 2.5 | CYP3A5*10 homozygote; nonexpressor for CYP3A5 |
Reference | GRCh38 38.1/141 |
Chromosome | 7 |
Position | 99650149 |
Gene | CYP3A5, ZSCAN25 |
is a | snp |
is | mentioned by |
dbSNP | rs41279854 |
dbSNP (classic) | rs41279854 |
ClinGen | rs41279854 |
ebi | rs41279854 |
HLI | rs41279854 |
Exac | rs41279854 |
Gnomad | rs41279854 |
Varsome | rs41279854 |
LitVar | rs41279854 |
Map | rs41279854 |
PheGenI | rs41279854 |
Biobank | rs41279854 |
1000 genomes | rs41279854 |
hgdp | rs41279854 |
ensembl | rs41279854 |
geneview | rs41279854 |
scholar | rs41279854 |
rs41279854 | |
pharmgkb | rs41279854 |
gwascentral | rs41279854 |
openSNP | rs41279854 |
23andMe | rs41279854 |
SNPshot | rs41279854 |
SNPdbe | rs41279854 |
MSV3d | rs41279854 |
GWAS Ctlg | rs41279854 |
Max Magnitude | 2.5 |
rs41279854, also known as 29748T>C or F446S, is a SNP in the CYP3A5 gene.
The rs41279854(G) allele defines the CYP3A5*10 variant, which is nonfunctional.