rs1085307938, CLCN2

N. diseases: 2
Source: ALL
Disease N. SNPs d DSI v DPI v Chr Position Consequence Alleles Class AFEXOME AFGENOME Score vda EI vda N. PMIDs First Ref. Last Ref.
Hyperaldosteronism, Familial, Type II
CUI: C1854107
Disease: Hyperaldosteronism, Familial, Type II
9 0.925 0.040 3 184359124 missense variant C/T snv 0.800 1.000 1 2018 2018
Conn Syndrome
CUI: C1384514
Disease: Conn Syndrome
25 0.925 0.040 3 184359124 missense variant C/T snv 0.010 1.000 1 2018 2018