rs12449782
From SNPedia
Orientation | plus |
Stabilized | plus |
Make rs12449782(A;A) |
Make rs12449782(A;G) |
Make rs12449782(G;G) |
Reference | GRCh38 38.1/141 |
Chromosome | 17 |
Position | 63498888 |
Gene | ACE |
is a | snp |
is | mentioned by |
dbSNP | rs12449782 |
dbSNP (classic) | rs12449782 |
ClinGen | rs12449782 |
ebi | rs12449782 |
HLI | rs12449782 |
Exac | rs12449782 |
Gnomad | rs12449782 |
Varsome | rs12449782 |
LitVar | rs12449782 |
Map | rs12449782 |
PheGenI | rs12449782 |
Biobank | rs12449782 |
1000 genomes | rs12449782 |
hgdp | rs12449782 |
ensembl | rs12449782 |
geneview | rs12449782 |
scholar | rs12449782 |
rs12449782 | |
pharmgkb | rs12449782 |
gwascentral | rs12449782 |
openSNP | rs12449782 |
23andMe | rs12449782 |
SNPshot | rs12449782 |
SNPdbe | rs12449782 |
MSV3d | rs12449782 |
GWAS Ctlg | rs12449782 |
GMAF | 0.4738 |
Max Magnitude | 0 |
[PMID 19787680] Identification of specific angiotensin-converting enzyme variants and haplotypes that confer risk and protection against type 2 diabetic nephropathy
[PMID 17376814] The G allele is associated with a slightly increased risk of diabetic nephropathy.
[PMID 20230274] Polymorphisms in the ACE and ADRB2 genes and risks of aging-associated phenotypes: the case of myocardial infarction.