Disease: Ventricular Fibrillation
Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs6795970
SCN10A
0.807 0.200 3 38725184 missense variant A/G snv 0.65 0.70 13
rs199473229
SCN5A
0.882 0.120 3 38560361 missense variant A/G snv 4
rs9388451 0.882 0.120 6 125769231 regulatory region variant T/A;C snv 3
rs199473574
SCN5A
0.925 0.120 3 38603951 missense variant C/T snv 2