rs386352319, KCNJ5

N. diseases: 8
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 Ten out of 28 (36 %) patients with PA displayed tumor mutations in KCNJ5 (p. G151R and L168R) while none were found in the corresponding non-tumor samples. 23778974 2013