rs1064795287, KCNH2

N. diseases: 2
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.
Long QT Syndrome
CUI: C0023976
Disease: Long QT Syndrome
349 0.925 0.120 7 150947683 frameshift variant GG/T delins 0.010 1.000 1 2018 2018
Sudden infant death syndrome
CUI: C0038644
Disease: Sudden infant death syndrome
68 0.925 0.120 7 150947683 frameshift variant GG/T delins 0.010 1.000 1 2018 2018