Source: UNIPROT

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 4
rs199473072
SCN5A
0.827 0.160 3 38613773 missense variant G/A snv 1.2E-05 8.4E-05 3
rs199473282
SCN5A
0.827 0.120 3 38551513 missense variant G/A;T snv 4.0E-06 3
rs41315493
SCN5A
0.851 0.120 3 38550521 missense variant C/A;T snv 6.6E-03; 9.7E-05 3
rs137854600
SCN5A
0.807 0.120 3 38551504 missense variant C/A;T snv 2
rs137854601
SCN5A
0.776 0.120 3 38551022 stop gained C/A;T snv 4.0E-06 2
rs137854611
SCN5A
0.882 0.120 3 38597787 missense variant G/A;C;T snv 4.0E-06 2
rs137854612
SCN5A
0.851 0.120 3 38560170 missense variant C/T snv 2
rs199473055
SCN5A
0.882 0.120 3 38630393 missense variant G/A;C snv 4.0E-06 2
rs199473062
SCN5A
0.827 0.120 3 38622401 stop gained C/A;G;T snv 4.1E-06 2
rs199473097
SCN5A
0.763 0.120 3 38606710 missense variant G/A snv 8.0E-06 7.0E-06 2
rs199473153
SCN5A
0.882 0.120 3 38597737 stop gained C/A;T snv 4.0E-06 2
rs199473207
SCN5A
0.882 0.120 3 38566555 missense variant G/A snv 2
rs199473225
SCN5A
0.851 0.120 3 38560397 missense variant G/A;C snv 2
rs199473266
SCN5A
0.882 0.120 3 38555697 missense variant G/C snv 2.0E-05 2
rs199473625
SCN5A
0.882 0.120 3 38551394 missense variant T/C snv 3.2E-05 7.0E-05 2
rs41261344
SCN5A
0.763 0.120 3 38575385 missense variant C/T snv 5.4E-03 2.2E-03 2
rs45546039
SCN5A
0.732 0.120 3 38613781 missense variant C/A;T snv 4.1E-06 2
rs1060499900
SCN5A
0.925 0.080 3 38551304 missense variant C/T snv 4.0E-06 1.4E-05 1
rs137854602
SCN5A
0.925 0.080 3 38555664 missense variant G/A snv 5.6E-05 1.4E-05 1
rs137854604
SCN5A
0.882 0.120 3 38551243 missense variant G/A snv 1.6E-05 7.0E-06 1
rs137854607
SCN5A
0.882 0.120 3 38554309 missense variant C/G;T snv 1
rs137854614
SCN5A
0.882 0.120 3 38550988 missense variant T/C snv 1
rs137854615
SCN5A
0.851 0.120 3 38550989 missense variant A/G snv 1
rs185638763
SCN5A
0.882 0.120 3 38599001 missense variant G/A;T snv 1.2E-05 1