Source: ALL

Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1805124
SCN5A
0.742 0.280 3 38603929 missense variant T/C snv 0.22 0.25 16
rs41261344
SCN5A
0.763 0.120 3 38575385 missense variant C/T snv 5.4E-03 2.2E-03 11
rs7626962
SCN5A
0.790 0.080 3 38579416 missense variant G/A;T snv 1.6E-05; 5.9E-03 10
rs11708996
SCN5A
0.925 0.120 3 38592432 intron variant G/C snv 0.11 6
rs7629265
SCN5A
0.882 0.080 3 38607330 intron variant C/T snv 2.3E-02 3
rs199473112
SCN5A
0.925 0.080 3 38605956 missense variant G/A;C snv 4.1E-06; 5.3E-05 2
rs199473260
SCN5A
0.925 0.120 3 38555720 missense variant T/C snv 1.6E-05 3.5E-05 2
rs199473324
SCN5A
0.925 0.120 3 38550748 missense variant A/G;T snv 4.0E-06 2
rs7374540
SCN5A
1.000 0.080 3 38592651 intron variant C/A snv 0.49 1
rs756805318
SCN5A
1.000 0.080 3 38633283 missense variant C/T snv 1.2E-05 2.8E-05 1
rs778337208
SCN5A
1.000 0.080 3 38622428 missense variant C/T snv 1.2E-05 1