rs758379595, CLCN2

N. diseases: 5
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.
Conn Syndrome
CUI: C1384514
Disease: Conn Syndrome
25 0.882 0.040 3 184359130 missense variant A/G;T snv 4.0E-06 0.700 0
Glucocortocoid-insensitive primary hyperaldosteronism
CUI: C4023208
Disease: Glucocortocoid-insensitive primary hyperaldosteronism
5 0.882 0.040 3 184359130 missense variant A/G;T snv 4.0E-06 0.700 0
Hyperaldosteronism, Familial, Type II
CUI: C1854107
Disease: Hyperaldosteronism, Familial, Type II
9 0.882 0.040 3 184359130 missense variant A/G;T snv 4.0E-06 0.700 0
Hypertensive disease
CUI: C0020538
Disease: Hypertensive disease
1085 0.882 0.040 3 184359130 missense variant A/G;T snv 4.0E-06 0.700 0
Hypokalemia
CUI: C0020621
Disease: Hypokalemia
7 0.882 0.040 3 184359130 missense variant A/G;T snv 4.0E-06 0.700 0