Source: CURATED ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
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
rs199473076
SCN5A
0.925 0.120 3 38609950 missense variant C/T snv 8.0E-06 2.8E-05 2
rs199473101
SCN5A
0.925 0.080 3 38606682 missense variant C/A;T snv 8.1E-06 2
rs199473124
SCN5A
0.851 0.120 3 38603902 missense variant A/T snv 8.0E-06 7.0E-06 2
rs199473133
SCN5A
0.882 0.120 3 38603747 missense variant G/A snv 3.1E-05 6.3E-05 2
rs199473147
SCN5A
0.925 0.120 3 38597889 missense variant G/A snv 8.8E-05 4.2E-05 2
rs199473157
SCN5A
0.925 0.120 3 38587522 missense variant C/T snv 2.0E-05 1.4E-05 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
rs199473207
SCN5A
0.882 0.120 3 38566555 missense variant G/A snv 2
rs199473246
SCN5A
0.925 0.120 3 38557234 missense variant C/G;T snv 2.0E-05 2
rs199473287
SCN5A
0.925 0.120 3 38551442 missense variant G/A snv 4.0E-06 2
rs199473292
SCN5A
0.925 0.080 3 38551391 missense variant C/G;T snv 2
rs199473293
SCN5A
0.925 0.120 3 38551373 missense variant C/G;T snv 4.0E-06 2
rs199473305
SCN5A
0.925 0.080 3 38551145 missense variant C/T snv 1.4E-05 2
rs199473554
SCN5A
0.925 0.080 3 38630392 missense variant C/T snv 2
rs199473556
SCN5A
0.851 0.120 3 38630342 missense variant G/A snv 2
rs199473565
SCN5A
0.882 0.120 3 38606743 missense variant C/T snv 4.0E-06 7.0E-06 2
rs199473573
SCN5A
0.925 0.120 3 38604007 missense variant A/C snv 1.6E-05 7.0E-06 2
rs199473620
SCN5A
1.000 0.080 3 38554372 stop gained C/A;T snv 2
rs199473623
SCN5A
0.882 0.120 3 38551486 missense variant C/T snv 1.2E-05 7.0E-06 2