rs7079

minus

Geno	Mag	Summary
(C;C)	0	common in clinvar

Make rs7079(A;A)

Make rs7079(A;C)

Reference

GRCh38 38.1/141

Chromosome

1

Position

230702585

Gene

AGT

is a	snp
is	mentioned by
dbSNP	rs7079
dbSNP (classic)	rs7079
ClinGen	rs7079
ebi	rs7079
HLI	rs7079
Exac	rs7079
Gnomad	rs7079
Varsome	rs7079
LitVar	rs7079
Map	rs7079
PheGenI	rs7079
Biobank	rs7079
1000 genomes	rs7079
hgdp	rs7079
ensembl	rs7079
geneview	rs7079
scholar	rs7079
google	rs7079
pharmgkb	rs7079
gwascentral	rs7079
openSNP	rs7079
23andMe	rs7079
SNPshot	rs7079
SNPdbe	rs7079
MSV3d	rs7079
GWAS Ctlg	rs7079

GMAF

0.2025

Max Magnitude

0

?

(A;A) (A;C) (C;C)

28

[PMID 21261619] Genetic variation in renin predicts the effects of thiazide diuretics

[PMID 21988197] Angiotensinogen gene haplotype is associated with the prevalence of Japanese non-alcoholic steatohepatitis

[PMID 17261659] Association between angiotensinogen, angiotensin II receptor genes, and blood pressure response to an angiotensin-converting enzyme inhibitor.

[PMID 21562941 ] Do genetic variants of the Renin-Angiotensin system predict blood pressure response to Renin-Angiotensin system-blocking drugs?: a systematic review of pharmacogenomics in the Renin-Angiotensin system.

[PMID 23943853 ] Human Angiotensinogen +11525 C/A Polymorphism Modulates Its Gene Expression Through MicroRNA Binding

[PMID 22858200] Angiotensinogen gene polymorphisms and food-intake behavior in young, normal female subjects in Japan.

ClinVar
Risk	rs7079(A;A)
Alt	rs7079(A;A)
Reference	Rs7079(C;C)
Significance	Non-pathogenic
Disease	Renal dysplasia
Variation	info
Gene	AGT
CLNDBN	Renal dysplasia
Reversed	1
HGVS	NC_000001.10:g.230838331G>T
CLNSRC
CLNACC	RCV000390829.1,

[PMID 30700972 ] A new model of the mechanism underlying lead poisoning: SNP in miRNA target region influence the AGT expression level.