rs3772622
From SNPedia
Orientation | minus |
Stabilized | minus |
Make rs3772622(A;A) |
Make rs3772622(A;G) |
Make rs3772622(G;G) |
Reference | GRCh38 38.1/141 |
Chromosome | 3 |
Position | 148717966 |
Gene | AGTR1 |
is a | snp |
is | mentioned by |
dbSNP | rs3772622 |
dbSNP (classic) | rs3772622 |
ClinGen | rs3772622 |
ebi | rs3772622 |
HLI | rs3772622 |
Exac | rs3772622 |
Gnomad | rs3772622 |
Varsome | rs3772622 |
LitVar | rs3772622 |
Map | rs3772622 |
PheGenI | rs3772622 |
Biobank | rs3772622 |
1000 genomes | rs3772622 |
hgdp | rs3772622 |
ensembl | rs3772622 |
geneview | rs3772622 |
scholar | rs3772622 |
rs3772622 | |
pharmgkb | rs3772622 |
gwascentral | rs3772622 |
openSNP | rs3772622 |
23andMe | rs3772622 |
SNPshot | rs3772622 |
SNPdbe | rs3772622 |
MSV3d | rs3772622 |
GWAS Ctlg | rs3772622 |
GMAF | 0.3682 |
Max Magnitude | 0 |
[PMID 19302184] Association between angiotensin II type 1 receptor polymorphisms and the occurrence of nonalcoholic fatty liver disease.
[PMID 23484035] Susceptibility and Gene Interaction Study of the Angiotensin II Type 1 Receptor (AGTR1) Gene Polymorphisms with Non-Alcoholic Fatty Liver Disease in a Multi-Ethnic Population