rs61751148, GML;CYP11B1

N. diseases: 1
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 In this study we investigated the presence of the mutation D147E of CYP11B2 in a group of 128 patients with primary aldosteronism, 68 patients with essential hypertension and increased corticosterone production and in 48 normal volunteers. 11275950 2001