rs2478545
From SNPedia
Orientation | minus |
Stabilized | minus |
Make rs2478545(C;C) |
Make rs2478545(C;T) |
Make rs2478545(T;T) |
Reference | GRCh38 38.1/141 |
Chromosome | 1 |
Position | 230708375 |
Gene | AGT |
is a | snp |
is | mentioned by |
dbSNP | rs2478545 |
dbSNP (classic) | rs2478545 |
ClinGen | rs2478545 |
ebi | rs2478545 |
HLI | rs2478545 |
Exac | rs2478545 |
Gnomad | rs2478545 |
Varsome | rs2478545 |
LitVar | rs2478545 |
Map | rs2478545 |
PheGenI | rs2478545 |
Biobank | rs2478545 |
1000 genomes | rs2478545 |
hgdp | rs2478545 |
ensembl | rs2478545 |
geneview | rs2478545 |
scholar | rs2478545 |
rs2478545 | |
pharmgkb | rs2478545 |
gwascentral | rs2478545 |
openSNP | rs2478545 |
23andMe | rs2478545 |
SNPshot | rs2478545 |
SNPdbe | rs2478545 |
MSV3d | rs2478545 |
GWAS Ctlg | rs2478545 |
GMAF | 0.3411 |
Max Magnitude | 0 |
? | (C;C) (C;T) (T;T) | 28 |
---|---|---|
|
[PMID 22739771] Genetic variation in the renin-angiotensin-aldosterone system is associated with cardiovascular risk factors and early mortality in established coronary heart disease
[PMID 19064790] Predictive genomics of cardioembolic stroke.
[PMID 19105203] An association analysis of Alzheimer disease candidate genes detects an ancestral risk haplotype clade in ACE and putative multilocus association between ACE, A2M, and LRRTM3.
[PMID 20537141] Maternal angiotensinogen (AGT) haplotypes, fetal renin (REN) haplotypes and risk of preeclampsia; estimation of gene-gene interaction from family-triad data.