Source: CLINVAR

Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Disease Score vda EI vda N. PMIDs First Ref. Last Ref.
dbSNP: rs121434500
rs121434500
SNTA1
0.851 0.120 20 33410203 missense variant G/A snv 2.0E-05 1.4E-05
CUI: C0004238
Disease: Atrial Fibrillation
Atrial Fibrillation 		0.700 0
dbSNP: rs199473260
rs199473260
SCN5A
0.925 0.120 3 38555720 missense variant T/C snv 1.6E-05 3.5E-05
CUI: C0004238
Disease: Atrial Fibrillation
Atrial Fibrillation 		0.700 0