Have questions? Visit https://www.reddit.com/r/SNPedia

rs7079

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs7079(A;A)
Make rs7079(A;C)
ReferenceGRCh38 38.1/141
Chromosome1
Position230702585
GeneAGT
is asnp
is mentioned by
dbSNPrs7079
dbSNP (old)rs7079
ClinGenrs7079
ebirs7079
HLIrs7079
Exacrs7079
Varsomers7079
Maprs7079
PheGenIrs7079
Biobankrs7079
1000 genomesrs7079
hgdprs7079
ensemblrs7079
gopubmedrs7079
geneviewrs7079
scholarrs7079
googlers7079
pharmgkbrs7079
gwascentralrs7079
openSNPrs7079
23andMers7079
23andMe allrs7079
SNP Nexus

SNPshotrs7079
SNPdbers7079
MSV3drs7079
GWAS Ctlgrs7079
GMAF0.2025
Max Magnitude0
? (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 21562941OA-icon.png] 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 23943853OA-icon.png] 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,