rs4986913
From SNPedia
Orientation | minus |
Stabilized | minus |
Geno | Mag | Summary |
---|---|---|
(C;C) | 0 | normal |
(C;T) | carrier of one CYP3A4*19 allele | |
(T;T) | CYP3A4*19 homozygote |
Reference | GRCh38 38.1/142 |
Chromosome | 7 |
Position | 99760836 |
Gene | CYP3A4 |
is a | snp |
is | mentioned by |
dbSNP | rs4986913 |
dbSNP (classic) | rs4986913 |
ClinGen | rs4986913 |
ebi | rs4986913 |
HLI | rs4986913 |
Exac | rs4986913 |
Gnomad | rs4986913 |
Varsome | rs4986913 |
LitVar | rs4986913 |
Map | rs4986913 |
PheGenI | rs4986913 |
Biobank | rs4986913 |
1000 genomes | rs4986913 |
hgdp | rs4986913 |
ensembl | rs4986913 |
geneview | rs4986913 |
scholar | rs4986913 |
rs4986913 | |
pharmgkb | rs4986913 |
gwascentral | rs4986913 |
openSNP | rs4986913 |
23andMe | rs4986913 |
SNPshot | rs4986913 |
SNPdbe | rs4986913 |
MSV3d | rs4986913 |
GWAS Ctlg | rs4986913 |
Max Magnitude | 0 |
? | (C;C) (C;T) (T;T) | 28 |
---|---|---|
|
rs4986913, also known as 1399C>T, 23237C>T or P467S, is a SNP in the CYP3A4 gene.
The rs4986913(T) allele defines the CYP3A4*19 variant.