rs17215437, KCNE3

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.
Familial Periodic Paralysis
CUI: C0030443
Disease: Familial Periodic Paralysis
10 0.851 0.200 11 74457316 missense variant C/T snv 3.0E-03 3.8E-03 0.020 1.000 2 2003 2004
periodic paralysis (finding)
CUI: C1279412
Disease: periodic paralysis (finding)
11 0.851 0.200 11 74457316 missense variant C/T snv 3.0E-03 3.8E-03 0.020 1.000 2 2003 2004
Hyperkalemic periodic paralysis
CUI: C0238357
Disease: Hyperkalemic periodic paralysis
30 0.851 0.200 11 74457316 missense variant C/T snv 3.0E-03 3.8E-03 0.010 1.000 1 2007 2007
Hypokalemic periodic paralysis
CUI: C0238358
Disease: Hypokalemic periodic paralysis
19 0.851 0.200 11 74457316 missense variant C/T snv 3.0E-03 3.8E-03 0.010 1.000 1 2002 2002