rs104894585, KCNJ2

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.
Andersen Syndrome
CUI: C1563715
Disease: Andersen Syndrome
38 0.851 0.120 17 70175263 missense variant C/G;T snv 0.810 1.000 11 2001 2015
Short QT Syndrome 3
CUI: C1865018
Disease: Short QT Syndrome 3
9 0.851 0.120 17 70175263 missense variant C/G;T snv 0.700 1.000 6 2005 2015
Tachycardia, Ventricular
CUI: C0042514
Disease: Tachycardia, Ventricular
31 0.851 0.120 17 70175263 missense variant C/G;T snv 0.020 1.000 2 2006 2007
Bidirectional tachycardia
CUI: C2930902
Disease: Bidirectional tachycardia
1 0.851 0.120 17 70175263 missense variant C/G;T snv 0.010 1.000 1 2006 2006
Syncope
CUI: C0039070
Disease: Syncope
45 0.851 0.120 17 70175263 missense variant C/G;T snv 0.010 1.000 1 2007 2007