Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs137854618
SCN5A
0.742 0.120 3 38566426 missense variant C/A;T snv 8.0E-06 15
rs45546039
SCN5A
0.732 0.120 3 38613781 missense variant C/A;T snv 4.1E-06 15
rs41261344
SCN5A
0.763 0.120 3 38575385 missense variant C/T snv 5.4E-03 2.2E-03 11
rs137854601
SCN5A
0.776 0.120 3 38551022 stop gained C/A;T snv 4.0E-06 10
rs199473097
SCN5A
0.763 0.120 3 38606710 missense variant G/A snv 8.0E-06 7.0E-06 9
rs757532106
SCN5A
0.763 0.120 3 38550500 stop gained G/A snv 4.5E-05 4.9E-05 9
rs199473119
SCN5A
0.790 0.120 3 38604035 missense variant G/A;T snv 8.4E-06; 4.2E-06 7
rs137854600
SCN5A
0.807 0.120 3 38551504 missense variant C/A;T snv 6
rs199473225
SCN5A
0.851 0.120 3 38560397 missense variant G/A;C snv 6
rs12720452
SCN5A
0.882 0.120 3 38603758 missense variant C/T snv 2.9E-04 2.9E-04 5
rs137854602
SCN5A
0.925 0.080 3 38555664 missense variant G/A snv 5.6E-05 1.4E-05 5
rs199473062
SCN5A
0.827 0.120 3 38622401 stop gained C/A;G;T snv 4.1E-06 5
rs199473072
SCN5A
0.827 0.160 3 38613773 missense variant G/A snv 1.2E-05 8.4E-05 5
rs199473282
SCN5A
0.827 0.120 3 38551513 missense variant G/A;T snv 4.0E-06 5
rs137854606
SCN5A
0.882 0.120 3 38604062 missense variant C/A snv 4
rs137854612
SCN5A
0.851 0.120 3 38560170 missense variant C/T snv 4
rs137854615
SCN5A
0.851 0.120 3 38550989 missense variant A/G snv 4
rs185638763
SCN5A
0.882 0.120 3 38599001 missense variant G/A;T snv 1.2E-05 4
rs199473124
SCN5A
0.851 0.120 3 38603902 missense variant A/T snv 8.0E-06 7.0E-06 4
rs199473153
SCN5A
0.882 0.120 3 38597737 stop gained C/A;T snv 4.0E-06 4
rs199473229
SCN5A
0.882 0.120 3 38560361 missense variant A/G snv 4
rs199473244
SCN5A
0.851 0.120 3 38557251 missense variant C/A snv 4
rs199473556
SCN5A
0.851 0.120 3 38630342 missense variant G/A snv 4
rs41315493
SCN5A
0.851 0.120 3 38550521 missense variant C/A;T snv 6.6E-03; 9.7E-05 4
rs765669597
SCN5A
0.851 0.120 3 38614063 stop gained A/C;T snv 4.7E-06 4