Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
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
rs1805124
SCN5A
0.742 0.280 3 38603929 missense variant T/C snv 0.22 0.25 16
rs104894580
KCNJ2
0.790 0.240 17 70175238 missense variant C/A;T snv 4.0E-06 7
rs199473605
SCN5A
0.851 0.120 3 38560374 missense variant C/G;T snv 4.8E-05; 4.0E-06 7
rs104894485
HCN4
0.882 0.080 15 73325378 missense variant C/T snv 3.6E-05 7.0E-06 4
rs121912516
KCNH2
0.882 0.120 7 150951721 missense variant C/G snv 3
rs199473561
SCN5A
0.882 0.120 3 38613769 missense variant G/A snv 9.1E-05 3.5E-05 3
rs199473284
SCN5A
0.925 0.120 3 38551487 stop gained G/A;C snv 8.0E-06 2
rs199473374
KCNJ2
1.000 0.080 17 70175340 missense variant T/C snv 1