rs5182

plus

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

Make rs5182(C;T)

Make rs5182(T;T)

Reference

GRCh38 38.1/141

Chromosome

3

Position

148741608

Gene

AGTR1

is a	snp
is	mentioned by
dbSNP	rs5182
dbSNP (classic)	rs5182
ClinGen	rs5182
ebi	rs5182
HLI	rs5182
Exac	rs5182
Gnomad	rs5182
Varsome	rs5182
LitVar	rs5182
Map	rs5182
PheGenI	rs5182
Biobank	rs5182
1000 genomes	rs5182
hgdp	rs5182
ensembl	rs5182
geneview	rs5182
scholar	rs5182
google	rs5182
pharmgkb	rs5182
gwascentral	rs5182
openSNP	rs5182
23andMe	rs5182
SNPshot	rs5182
SNPdbe	rs5182
MSV3d	rs5182
GWAS Ctlg	rs5182

GMAF

0.4747

Max Magnitude

0

?

(C;C) (C;T) (T;T)

28

rs5182 (573C/T) is a SNP within the AGTR1 (Angiotensin II receptor type 1).

[PMID 18347611] among 4,096 hypertensive subjects, the CT/CC genotypes were associated with reduced risk of heart attack among those treated with ACE inhibitors

[PMID 21671168] Association of polymorphisms in angiotensin II receptor genes with aldosterone-producing adenoma

[PMID 22508051] Renin-Angiotensin-aldosterone system gene polymorphisms and coronary artery disease: detection of gene-gene and gene-environment interactions

[PMID 21846682] Association of angiotensin II type 1-receptor gene polymorphisms with the risk of developing hypertension in Mexican individuals.

[PMID 24622918] Renin-Angiotensin System Genetic Polymorphisms and Brain White Matter Lesions in Older Australians

[PMID 24722536 ] Relationship of renin-angiotensin-aldosterone system polymorphisms and phenotypes to mortality in Chinese coronary atherosclerosis patients

ClinVar
Risk	rs5182(T;T)
Alt	rs5182(T;T)
Reference	Rs5182(C;C)
Significance	Non-pathogenic
Disease	not specified Renal dysplasia
Variation	info
Gene	AGTR1
CLNDBN	not specified Renal dysplasia
Reversed	0
HGVS	NC_000003.11:g.148459395C>T
CLNSRC
CLNACC	RCV000248373.1, RCV000392743.1,