rs1926723
From SNPedia
Orientation | minus |
Stabilized | minus |
Geno | Mag | Summary |
---|---|---|
(A;A) | 0 | common in clinvar |
Make rs1926723(A;G) |
Make rs1926723(G;G) |
Reference | GRCh38 38.1/141 |
Chromosome | 1 |
Position | 230704350 |
Gene | AGT |
is a | snp |
is | mentioned by |
dbSNP | rs1926723 |
dbSNP (classic) | rs1926723 |
ClinGen | rs1926723 |
ebi | rs1926723 |
HLI | rs1926723 |
Exac | rs1926723 |
Gnomad | rs1926723 |
Varsome | rs1926723 |
LitVar | rs1926723 |
Map | rs1926723 |
PheGenI | rs1926723 |
Biobank | rs1926723 |
1000 genomes | rs1926723 |
hgdp | rs1926723 |
ensembl | rs1926723 |
geneview | rs1926723 |
scholar | rs1926723 |
rs1926723 | |
pharmgkb | rs1926723 |
gwascentral | rs1926723 |
openSNP | rs1926723 |
23andMe | rs1926723 |
SNPshot | rs1926723 |
SNPdbe | rs1926723 |
MSV3d | rs1926723 |
GWAS Ctlg | rs1926723 |
GMAF | 0.1442 |
Max Magnitude | 0 |
? | (A;A) (A;G) (G;G) | 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
ClinVar | |
---|---|
Risk | rs1926723(C;C) rs1926723(G;G) rs1926723(T;T) |
Alt | rs1926723(C;C) rs1926723(G;G) rs1926723(T;T) |
Reference | Rs1926723(A;A) |
Significance | Non-pathogenic |
Disease | Renal dysplasia |
Variation | info |
Gene | AGT |
CLNDBN | Renal dysplasia |
Reversed | 1 |
HGVS | NC_000001.10:g.230840096T>C |
CLNSRC | |
CLNACC | RCV000335269.1, |