rs11708996, SCN5A

N. diseases: 6
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)
201 0.925 0.120 3 38592432 intron variant G/C snv 0.11 0.820 1.000 3 2013 2018
Electrocardiogram: P-R interval
CUI: C0429087
Disease: Electrocardiogram: P-R interval
138 0.925 0.120 3 38592432 intron variant G/C snv 0.11 0.800 1.000 3 2010 2019
Heart Function Tests
CUI: C0018803
Disease: Heart Function Tests
27 0.925 0.120 3 38592432 intron variant G/C snv 0.11 0.700 1.000 1 2010 2010
QRS complex feature
CUI: C0429097
Disease: QRS complex feature
69 0.925 0.120 3 38592432 intron variant G/C snv 0.11 0.700 1.000 1 2016 2016
QT interval feature (observable entity)
CUI: C0429028
Disease: QT interval feature (observable entity)
226 0.925 0.120 3 38592432 intron variant G/C snv 0.11 0.700 1.000 1 2014 2014
Atrial Fibrillation
CUI: C0004238
Disease: Atrial Fibrillation
584 0.925 0.120 3 38592432 intron variant G/C snv 0.11 0.010 1.000 1 2014 2014