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.
Romano-Ward Syndrome
CUI: C0035828
Disease: Romano-Ward Syndrome
232 0.821 0.107 11 2583535 missense variant C/A,G,T snp 0.840 1.000 12 1996 2015
Long QT Syndrome
CUI: C0023976
Disease: Long QT Syndrome
236 0.821 0.107 11 2583535 missense variant C/A,G,T snp 0.730 1.000 7 1999 2017
Congenital long QT syndrome
CUI: C1141890
Disease: Congenital long QT syndrome
223 0.821 0.107 11 2583535 missense variant C/A,G,T snp 0.720 1.000 14 1996 2012
LONG QT SYNDROME 1/2, DIGENIC (disorder)
418 0.821 0.107 11 2583535 missense variant C/A,G,T snp 0.700 6 1996 2010
LONG QT SYNDROME 1, ACQUIRED, SUSCEPTIBILITY TO
192 0.821 0.107 11 2583535 missense variant C/A,G,T snp 0.700 6 1996 2010
cardiac event
CUI: C0741923
Disease: cardiac event
18 0.821 0.107 11 2583535 missense variant C/A,G,T snp 0.040 1.000 4 2006 2015
Fetal Distress
CUI: C0015930
Disease: Fetal Distress
1 0.821 0.107 11 2583535 missense variant C/A,G,T snp 0.010 1.000 1 2006 2006