rs4986908
From SNPedia
Orientation | minus |
Stabilized | minus |
Geno | Mag | Summary |
---|---|---|
(A;A) | CYP3A4*_14313G>A(E174H) homozygote | |
(A;G) | carrier of one CYP3A4*_14313G>A(E174H) allele | |
(G;G) | 0 | normal |
Reference | GRCh38 38.1/141 |
Chromosome | 7 |
Position | 99769769 |
Gene | CYP3A4 |
is a | snp |
is | mentioned by |
dbSNP | rs4986908 |
dbSNP (classic) | rs4986908 |
ClinGen | rs4986908 |
ebi | rs4986908 |
HLI | rs4986908 |
Exac | rs4986908 |
Gnomad | rs4986908 |
Varsome | rs4986908 |
LitVar | rs4986908 |
Map | rs4986908 |
PheGenI | rs4986908 |
Biobank | rs4986908 |
1000 genomes | rs4986908 |
hgdp | rs4986908 |
ensembl | rs4986908 |
geneview | rs4986908 |
scholar | rs4986908 |
rs4986908 | |
pharmgkb | rs4986908 |
gwascentral | rs4986908 |
openSNP | rs4986908 |
23andMe | rs4986908 |
SNPshot | rs4986908 |
SNPdbe | rs4986908 |
MSV3d | rs4986908 |
GWAS Ctlg | rs4986908 |
GMAF | 0.002296 |
Max Magnitude | 0 |
rs4986908 is a SNP in the CYP3A4 gene.
The rs4986908(A) allele defines the CYP3A4*_14313G>A(E174H) variant.
? | (A;G) (G;G) | |
---|---|---|
|