Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs137854618
SCN5A
0.742 0.120 3 38566426 missense variant C/A;T snv 8.0E-06 15
rs1415058026
KCNQ1
11 2588755 missense variant A/G snv 4.0E-06 1
rs143624519
MAPT
0.724 0.240 17 45991484 missense variant G/A;T snv 1.5E-03; 1.2E-05 17
rs147750704
KCNJ2
0.925 0.080 17 70175316 missense variant G/A snv 1.6E-04 7.0E-05 3
rs150821281
PKP2
0.827 0.080 12 32878461 missense variant G/A snv 2.3E-03 2.5E-03 7
rs1800172
KCNQ1-AS1 ; KCNQ1
0.925 0.120 11 2847899 missense variant G/A;T snv 6.2E-03 4
rs1800562
LOC108783645 ; HFE
0.435 0.880 6 26092913 missense variant G/A snv 3.3E-02 3.8E-02 262
rs1805123
KCNH2
0.724 0.280 7 150948446 missense variant T/A;C;G snv 1.3E-05; 0.18; 8.4E-06 18
rs1805127
KCNE1
0.732 0.240 21 34449523 missense variant T/C snv 0.64 2.0E-04 17
rs1805128
KCNE1
0.776 0.160 21 34449382 missense variant C/T snv 9.4E-03 10
rs184442491
SCN5A
1.000 0.120 3 38603888 missense variant C/A snv 2.1E-04 7.7E-04 2
rs1860561
ATP2A2
0.851 0.080 12 110345436 intron variant G/A snv 0.19 5
rs199472708
KCNQ1
0.882 0.080 11 2572015 missense variant G/A snv 4
rs199472762
KCNQ1
1.000 0.120 11 2583540 missense variant C/T snv 2
rs199472936
KCNH2
0.882 0.120 7 150951592 missense variant C/A;T snv 5
rs199473024
KCNH2
7 150947362 missense variant T/C snv 7.0E-06 2
rs199473142
SCN5A
1.000 0.120 3 38597952 missense variant C/T snv 2.1E-05 2
rs199473225
SCN5A
0.851 0.120 3 38560397 missense variant G/A;C snv 6
rs199473256
SCN5A
1.000 0.120 3 38556460 missense variant A/C;G snv 2
rs199473283
SCN5A
1.000 0.120 3 38551495 missense variant C/A;G;T snv 4.0E-05 2
rs199473310
SCN5A
1.000 0.120 3 38551076 missense variant T/A;C;G snv 2
rs199473387
KCNJ2
1.000 0.120 17 70175952 missense variant A/C;G snv 2
rs199473401
KCNQ1
0.925 0.120 11 2570722 missense variant T/C snv 4
rs199473405
KCNQ1
1.000 0.120 11 2585249 missense variant A/G snv 2
rs199473580
SCN5A
1.000 0.120 3 38597926 missense variant G/A snv 1.6E-05 7.0E-06 2