rs10428132, SCN10A

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.
Brugada Syndrome (disorder)
CUI: C1142166
Disease: Brugada Syndrome (disorder)
201 0.925 0.120 3 38736063 intron variant T/G snv 0.67 0.830 1.000 4 2013 2018
Atrial Fibrillation
CUI: C0004238
Disease: Atrial Fibrillation
584 0.925 0.120 3 38736063 intron variant T/G snv 0.67 0.010 1.000 1 2014 2014