Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs104894230
HRAS ; LRRC56
0.564 0.600 11 534288 missense variant C/A;G;T snv 73
rs104894228
LRRC56 ; HRAS
0.605 0.560 11 534286 missense variant C/A;G;T snv 48
rs10757278
CDKN2B-AS1
0.620 0.520 9 22124478 intron variant A/G snv 0.40 44
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
rs2200733 0.752 0.240 4 110789013 intergenic variant C/T snv 0.18 12
rs60682848
LMNA
0.790 0.200 1 156134838 stop gained C/T snv 7.0E-06 11
rs120074192
KCNQ1
0.763 0.120 11 2527959 missense variant A/G snv 10
rs3825214
TBX5
0.851 0.080 12 114357638 intron variant G/A snv 0.77 8
rs794728708
RYR2
0.827 0.120 1 237377386 missense variant G/A;T snv 8
rs199473225
SCN5A
0.851 0.120 3 38560397 missense variant G/A;C snv 6
rs104894021
KCNH2
0.851 0.120 7 150951629 missense variant G/C;T snv 5
rs104894584
KCNJ2
0.851 0.120 17 70175553 missense variant G/A snv 5
rs1860561
ATP2A2
0.851 0.080 12 110345436 intron variant G/A snv 0.19 5
rs199472936
KCNH2
0.882 0.120 7 150951592 missense variant C/A;T snv 5
rs121912507
KCNH2
0.882 0.120 7 150951511 missense variant C/G;T snv 4
rs137854606
SCN5A
0.882 0.120 3 38604062 missense variant C/A snv 4
rs199472708
KCNQ1
0.882 0.080 11 2572015 missense variant G/A snv 4
rs199473401
KCNQ1
0.925 0.120 11 2570722 missense variant T/C snv 4
rs199473604
SCN5A
0.882 0.120 3 38560394 missense variant G/T snv 4
rs58327533
LMNA
1.000 0.120 1 156114991 missense variant C/G;T snv 4
rs104893714
SSUH2 ; CAV3
0.925 0.120 3 8745701 missense variant T/G snv 3
rs104893907
NKX2-5
1.000 5 173232776 stop gained A/C;T snv 3
rs120074195
KCNQ1
0.925 0.120 11 2572984 missense variant G/A;C snv 3
rs121918602
RYR2
0.925 0.120 1 237454396 missense variant T/C snv 3