Source: CURATED ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs45546039
SCN5A
0.732 0.120 3 38613781 missense variant C/A;T snv 4.1E-06 10
rs137854618
SCN5A
0.742 0.120 3 38566426 missense variant C/A;T snv 8.0E-06 8
rs199473119
SCN5A
0.790 0.120 3 38604035 missense variant G/A;T snv 8.4E-06; 4.2E-06 7
rs137854601
SCN5A
0.776 0.120 3 38551022 stop gained C/A;T snv 4.0E-06 6
rs137854600
SCN5A
0.807 0.120 3 38551504 missense variant C/A;T snv 4
rs137854612
SCN5A
0.851 0.120 3 38560170 missense variant C/T snv 4
rs199473282
SCN5A
0.827 0.120 3 38551513 missense variant G/A;T snv 4.0E-06 4
rs765669597
SCN5A
0.851 0.120 3 38614063 stop gained A/C;T snv 4.7E-06 4
rs137854606
SCN5A
0.882 0.120 3 38604062 missense variant C/A snv 3
rs137854611
SCN5A
0.882 0.120 3 38597787 missense variant G/A;C;T snv 4.0E-06 3
rs199473062
SCN5A
0.827 0.120 3 38622401 stop gained C/A;G;T snv 4.1E-06 3
rs199473153
SCN5A
0.882 0.120 3 38597737 stop gained C/A;T snv 4.0E-06 3
rs199473225
SCN5A
0.851 0.120 3 38560397 missense variant G/A;C snv 3
rs199473266
SCN5A
0.882 0.120 3 38555697 missense variant G/C snv 2.0E-05 3
rs41315493
SCN5A
0.851 0.120 3 38550521 missense variant C/A;T snv 6.6E-03; 9.7E-05 3
rs137854609
SCN5A
0.882 0.120 3 38581170 missense variant C/A;T snv 7.9E-05 2
rs199473045
SCN5A
0.925 0.120 3 38633228 missense variant C/A;T snv 8.0E-06; 2.5E-04 2
rs199473055
SCN5A
0.882 0.120 3 38630393 missense variant G/A;C snv 4.0E-06 2
rs199473058
SCN5A
0.925 0.080 3 38630341 missense variant C/T snv 4.0E-06 2
rs199473070
SCN5A
0.925 0.120 3 38613811 missense variant A/G;T snv 2
rs199473101
SCN5A
0.925 0.080 3 38606682 missense variant C/A;T snv 8.1E-06 2
rs199473169
SCN5A
0.925 0.080 3 38585821 missense variant T/G snv 2
rs199473172
SCN5A
0.925 0.080 3 38585800 missense variant C/A;T snv 4.0E-06 2
rs199473181
SCN5A
0.925 0.120 3 38581265 missense variant C/A;T snv 4.1E-06 2
rs199473204
SCN5A
0.925 0.120 3 38566576 stop gained C/A;T snv 4.0E-06 2