rs1311839715, KCNJ18

N. diseases: 3
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.
Hyperthyroidism
CUI: C0020550
Disease: Hyperthyroidism
27 0.882 0.200 17 21703291 missense variant G/C snv 7.0E-06 0.010 1.000 1 2016 2016
Hypokalemic periodic paralysis
CUI: C0238358
Disease: Hypokalemic periodic paralysis
19 0.882 0.200 17 21703291 missense variant G/C snv 7.0E-06 0.010 1.000 1 2016 2016
Hypokalemic periodic paralysis type 1
CUI: C3714580
Disease: Hypokalemic periodic paralysis type 1
24 0.882 0.200 17 21703291 missense variant G/C snv 7.0E-06 0.010 1.000 1 2016 2016