rs11568020
From SNPedia
Orientation | minus |
Stabilized | minus |
Geno | Mag | Summary |
---|---|---|
(G;G) | 0 | common in clinvar |
Make rs11568020(A;A) |
Make rs11568020(A;G) |
Reference | GRCh38.p7 38.3/150 |
Chromosome | 1 |
Position | 230714272 |
Gene | AGT |
is a | snp |
is | mentioned by |
dbSNP | rs11568020 |
dbSNP (classic) | rs11568020 |
ClinGen | rs11568020 |
ebi | rs11568020 |
HLI | rs11568020 |
Exac | rs11568020 |
Gnomad | rs11568020 |
Varsome | rs11568020 |
LitVar | rs11568020 |
Map | rs11568020 |
PheGenI | rs11568020 |
Biobank | rs11568020 |
1000 genomes | rs11568020 |
hgdp | rs11568020 |
ensembl | rs11568020 |
geneview | rs11568020 |
scholar | rs11568020 |
rs11568020 | |
pharmgkb | rs11568020 |
gwascentral | rs11568020 |
openSNP | rs11568020 |
23andMe | rs11568020 |
SNPshot | rs11568020 |
SNPdbe | rs11568020 |
MSV3d | rs11568020 |
GWAS Ctlg | rs11568020 |
Max Magnitude | 0 |
? | (A;A) (A;G) (G;G) | 28 |
---|---|---|
|
[PMID 28361007] Association of angiotensinogen gene SNPs and haplotypes with risk of hypertension in eastern Indian population.
ClinVar | |
---|---|
Risk | rs11568020(A;A) rs11568020(T;T) |
Alt | rs11568020(A;A) rs11568020(T;T) |
Reference | Rs11568020(G;G) |
Significance | Probable-non-pathogenic |
Disease | Renal dysplasia |
Variation | info |
Gene | AGT |
CLNDBN | Renal dysplasia |
Reversed | 1 |
HGVS | NC_000001.10:g.230850018C>T |
CLNSRC | |
CLNACC | RCV000342647.1, |