rs1553857113, CLCN2

N. diseases: 4
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 0.882 0.040 3 184359119 missense variant A/T snv 0.800 1.000 2 2018 2018
Conn Syndrome
CUI: C1384514
Disease: Conn Syndrome
25 0.882 0.040 3 184359119 missense variant A/T snv 0.700 0
Glucocortocoid-insensitive primary hyperaldosteronism
CUI: C4023208
Disease: Glucocortocoid-insensitive primary hyperaldosteronism
5 0.882 0.040 3 184359119 missense variant A/T snv 0.700 0
Hypertensive disease
CUI: C0020538
Disease: Hypertensive disease
1085 0.882 0.040 3 184359119 missense variant A/T snv 0.700 0