rs55951658
From SNPedia
Orientation | plus |
Stabilized | plus |
Geno | Mag | Summary |
---|---|---|
(C;C) | CYP3A4*4 homozygote | |
(C;T) | carrier of one CYP3A4*4 allele | |
(T;T) | 0 | normal |
Reference | GRCh38 38.1/141 |
Chromosome | 7 |
Position | 99770202 |
Gene | CYP3A4 |
is a | snp |
is | mentioned by |
dbSNP | rs55951658 |
dbSNP (classic) | rs55951658 |
ClinGen | rs55951658 |
ebi | rs55951658 |
HLI | rs55951658 |
Exac | rs55951658 |
Gnomad | rs55951658 |
Varsome | rs55951658 |
LitVar | rs55951658 |
Map | rs55951658 |
PheGenI | rs55951658 |
Biobank | rs55951658 |
1000 genomes | rs55951658 |
hgdp | rs55951658 |
ensembl | rs55951658 |
geneview | rs55951658 |
scholar | rs55951658 |
rs55951658 | |
pharmgkb | rs55951658 |
gwascentral | rs55951658 |
openSNP | rs55951658 |
23andMe | rs55951658 |
SNPshot | rs55951658 |
SNPdbe | rs55951658 |
MSV3d | rs55951658 |
GWAS Ctlg | rs55951658 |
Max Magnitude | 0 |
rs55951658, also known as 352A>G, 13871A>G or I118V, is a SNP in the CYP3A4 gene.
The rs55951658(C) allele defines the CYP3A4*4 variant.