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.
Brugada Syndrome (disorder)
CUI: C1142166
Disease: Brugada Syndrome (disorder)
292 0.756 0.107 3 38551513 missense variant G/A,T snp 4.0E-06 0.840 1.000 16 1998 2017
CARDIAC CONDUCTION DEFECT, NONSPECIFIC (disorder)
219 0.756 0.107 3 38551513 missense variant G/A,T snp 4.0E-06 0.700 4 1998 2011
LONG QT SYNDROME 2/3, DIGENIC
CUI: C3276240
Disease: LONG QT SYNDROME 2/3, DIGENIC
367 0.756 0.107 3 38551513 missense variant G/A,T snp 4.0E-06 0.700 0
Cardiac Conduction Defect, Nonprogressive
10 0.756 0.107 3 38551513 missense variant G/A,T snp 4.0E-06 0.700 0
Heart Block, Nonprogressive
CUI: C1861983
Disease: Heart Block, Nonprogressive
11 0.756 0.107 3 38551513 missense variant G/A,T snp 4.0E-06 0.700 0
LONG QT SYNDROME 3, ACQUIRED, SUSCEPTIBILITY TO (finding)
141 0.756 0.107 3 38551513 missense variant G/A,T snp 4.0E-06 0.700 0
LONG QT SYNDROME 3
CUI: C1859062
Disease: LONG QT SYNDROME 3
148 0.756 0.107 3 38551513 missense variant G/A,T snp 4.0E-06 0.700 0
Hereditary bundle branch system defect
11 0.756 0.107 3 38551513 missense variant G/A,T snp 4.0E-06 0.700 0
LONG QT SYNDROME 3/6, DIGENIC Disorder
151 0.756 0.107 3 38551513 missense variant G/A,T snp 4.0E-06 0.700 0
Long QT Syndrome
CUI: C0023976
Disease: Long QT Syndrome
236 0.756 0.107 3 38551513 missense variant G/A,T snp 4.0E-06 0.010 1.000 1 2008 2008