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rs1926723

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs1926723(A;G)
Make rs1926723(G;G)
ReferenceGRCh38 38.1/141
Chromosome1
Position230704350
GeneAGT
is asnp
is mentioned by
dbSNPrs1926723
dbSNP (classic)rs1926723
ClinGenrs1926723
ebirs1926723
HLIrs1926723
Exacrs1926723
Gnomadrs1926723
Varsomers1926723
LitVarrs1926723
Maprs1926723
PheGenIrs1926723
Biobankrs1926723
1000 genomesrs1926723
hgdprs1926723
ensemblrs1926723
geneviewrs1926723
scholarrs1926723
googlers1926723
pharmgkbrs1926723
gwascentralrs1926723
openSNPrs1926723
23andMers1926723
SNPshotrs1926723
SNPdbers1926723
MSV3drs1926723
GWAS Ctlgrs1926723
GMAF0.1442
Max Magnitude0
? (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,