rs1926723

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
google	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,