Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs16847548 0.807 0.120 1 162065484 upstream gene variant T/C snv 0.22 8
rs4657139 0.925 0.120 1 162060117 intergenic variant A/T snv 0.48 3
rs398124647
CALM2
0.807 0.120 2 47161851 missense variant T/A;C snv 6
rs398124650
CALM2
0.882 0.120 2 47161744 missense variant C/G;T snv 3
rs137854601
SCN5A
0.776 0.120 3 38551022 stop gained C/A;T snv 4.0E-06 10
rs199473225
SCN5A
0.851 0.120 3 38560397 missense variant G/A;C snv 6
rs199473103
SCN5A
0.925 0.120 3 38606102 missense variant A/G snv 3
rs199473317
SCN5A
0.882 0.120 3 38551003 missense variant T/C snv 3
rs199473631
SCN5A
0.925 0.120 3 38551085 missense variant C/T snv 3
rs199473051
SCN5A
0.925 0.120 3 38633058 missense variant C/T snv 2
rs794728846
SCN5A
0.925 0.120 3 38620972 splice acceptor variant C/T snv 2
rs794728879
SCN5A
0.925 0.120 3 38560146 splice donor variant C/A;G;T snv 2
rs1480085793
SCN5A
1.000 0.120 3 38620919 stop gained G/A snv 4.0E-06 1
rs770088052
SCN5A
1.000 0.120 3 38581182 missense variant C/A;T snv 4.2E-06; 8.4E-06 1
rs780405533
SCN5A
1.000 0.120 3 38560221 stop gained C/A;T snv 3.6E-05 2.1E-05 1
rs554903493
SLCO6A1
1.000 0.120 5 102419940 missense variant G/A snv 8.2E-06 2
rs1805123
KCNH2
0.724 0.280 7 150948446 missense variant T/A;C;G snv 1.3E-05; 0.18; 8.4E-06 18
rs767910122
KCNH2
0.724 0.280 7 150948446 frameshift variant -/GTCCG ins 4.4E-05 17
rs794728448
KCNH2
0.724 0.280 7 150948445 frameshift variant CT/G delins 17
rs199472910
KCNH2
0.827 0.120 7 150952508 missense variant G/A snv 1.2E-05 5
rs199472936
KCNH2
0.882 0.120 7 150951592 missense variant C/A;T snv 5
rs199473428
KCNH2
0.851 0.120 7 150951643 missense variant C/A;G;T snv 8.0E-06 4
rs199472944
KCNH2
0.882 0.120 7 150951552 missense variant G/A snv 3
rs199472990
KCNH2
0.882 0.120 7 150950312 missense variant G/A snv 7.0E-06 3
rs199473522
KCNH2
0.882 0.120 7 150951583 missense variant C/T snv 3