rs4986907
From SNPedia
Orientation | minus |
Stabilized | minus |
Geno | Mag | Summary |
---|---|---|
(A;A) | CYP3A4*15A homozygote | |
(A;G) | carrier of one CYP3A4*15A allele | |
(G;G) | 0 | normal |
Reference | GRCh38 38.1/142 |
Chromosome | 7 |
Position | 99769804 |
Gene | CYP3A4 |
is a | snp |
is | mentioned by |
dbSNP | rs4986907 |
dbSNP (classic) | rs4986907 |
ClinGen | rs4986907 |
ebi | rs4986907 |
HLI | rs4986907 |
Exac | rs4986907 |
Gnomad | rs4986907 |
Varsome | rs4986907 |
LitVar | rs4986907 |
Map | rs4986907 |
PheGenI | rs4986907 |
Biobank | rs4986907 |
1000 genomes | rs4986907 |
hgdp | rs4986907 |
ensembl | rs4986907 |
geneview | rs4986907 |
scholar | rs4986907 |
rs4986907 | |
pharmgkb | rs4986907 |
gwascentral | rs4986907 |
openSNP | rs4986907 |
23andMe | rs4986907 |
SNPshot | rs4986907 |
SNPdbe | rs4986907 |
MSV3d | rs4986907 |
GWAS Ctlg | rs4986907 |
GMAF | 0.004132 |
Max Magnitude | 0 |
? | (A;A) (A;G) (G;G) | 28 |
---|---|---|
|
rs4986907, also known as 485G>A, 14269G>A or R162Q, is a SNP in the CYP3A4 gene.
The rs4986907(A) allele defines the CYP3A4*15A variant.
[PMID 17615053] Polymorphisms in the cytochrome P450 genes CYP1A2, CYP1B1, CYP3A4, CYP3A5, CYP11A1, CYP17A1, CYP19A1 and colorectal cancer risk.