rs3772616, AGTR1

N. diseases: 2
Disease: Conn Syndrome ×
Source: ALL
Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
Conn Syndrome
CUI: C1384514
Disease: Conn Syndrome
0.010 GeneticVariation BEFREE The AGTR1 rs3772616 polymorphism can be considered as a hereditary marker for primary aldosteronism, and in the Chinese Han population the rs5193 G allele seems to predispose to it only in women. 25172908 2015