rs67784355
From SNPedia
Orientation | plus |
Stabilized | plus |
Geno | Mag | Summary |
---|---|---|
(A;A) | CYP3A4*11 homozygote | |
(A;G) | carrier of one CYP3A4*11 allele | |
(G;G) | 0 | normal |
Reference | GRCh38 38.1/141 |
Chromosome | 7 |
Position | 99762206 |
Gene | CYP3A4 |
is a | snp |
is | mentioned by |
dbSNP | rs67784355 |
dbSNP (classic) | rs67784355 |
ClinGen | rs67784355 |
ebi | rs67784355 |
HLI | rs67784355 |
Exac | rs67784355 |
Gnomad | rs67784355 |
Varsome | rs67784355 |
LitVar | rs67784355 |
Map | rs67784355 |
PheGenI | rs67784355 |
Biobank | rs67784355 |
1000 genomes | rs67784355 |
hgdp | rs67784355 |
ensembl | rs67784355 |
geneview | rs67784355 |
scholar | rs67784355 |
rs67784355 | |
pharmgkb | rs67784355 |
gwascentral | rs67784355 |
openSNP | rs67784355 |
23andMe | rs67784355 |
SNPshot | rs67784355 |
SNPdbe | rs67784355 |
MSV3d | rs67784355 |
GWAS Ctlg | rs67784355 |
Max Magnitude | 0 |
rs67784355, also known as 1088C>T, 21867C>T or T363M, is a SNP in the CYP3A4 gene.
The rs67784355(A) allele defines the CYP3A4*11 variant.