rs104894021, KCNH2

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.
Short QT Syndrome 1
CUI: C1865020
Disease: Short QT Syndrome 1
6 0.851 0.120 7 150951629 missense variant G/C;T snv 0.800 1.000 2 2004 2005
Short Qt Syndrome
CUI: C2348199
Disease: Short Qt Syndrome
5 0.851 0.120 7 150951629 missense variant G/C;T snv 0.080 1.000 8 2005 2019
Atrial Fibrillation
CUI: C0004238
Disease: Atrial Fibrillation
584 0.851 0.120 7 150951629 missense variant G/C;T snv 0.010 1.000 1 2014 2014
Cardiac Arrhythmia
CUI: C0003811
Disease: Cardiac Arrhythmia
111 0.851 0.120 7 150951629 missense variant G/C;T snv 0.010 1.000 1 2005 2005
Familial (FPAH)
CUI: C1611743
Disease: Familial (FPAH)
276 0.851 0.120 7 150951629 missense variant G/C;T snv 0.010 1.000 1 2005 2005