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rs5182

From SNPedia

Orientationplus
Stabilizedplus
Make rs5182(C;C)
Make rs5182(C;T)
Make rs5182(T;T)
ReferenceGRCh38 38.1/141
Chromosome3
Position148741608
GeneAGTR1
is asnp
is mentioned by
dbSNPrs5182
ebirs5182
HLIrs5182
Exacrs5182
Varsomers5182
Maprs5182
PheGenIrs5182
hapmaprs5182
1000 genomesrs5182
hgdprs5182
ensemblrs5182
gopubmedrs5182
geneviewrs5182
scholarrs5182
googlers5182
pharmgkbrs5182
gwascentralrs5182
openSNPrs5182
23andMers5182
23andMe allrs5182
SNP Nexus

SNPshotrs5182
SNPdbers5182
MSV3drs5182
GWAS Ctlgrs5182
GMAF0.4747
Max Magnitude
? (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.


GET Evidence
rs5182
aa_change
aa_change_short
impact pharmacogenetic
qualified_impact Insufficiently evaluated pharmacogenetic
overall_frequency 0.374698
summary



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


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