Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs104893714
SSUH2 ; CAV3
0.925 0.120 3 8745701 missense variant T/G snv 3
rs1316189390
HCN4 ; LOC105370890
1.000 0.040 15 73343594 missense variant T/C snv 4.0E-06 2
rs7219669 17 70525720 intergenic variant G/T snv 0.45 1
rs199473387
KCNJ2
1.000 0.120 17 70175952 missense variant A/C;G snv 2
rs104894584
KCNJ2
0.851 0.120 17 70175553 missense variant G/A snv 5
rs147750704
KCNJ2
0.925 0.080 17 70175316 missense variant G/A snv 1.6E-04 7.0E-05 3
rs5443
CDCA3 ; GNB3
0.532 0.760 12 6845711 synonymous variant C/T snv 0.36 0.44 106
rs104894503
TPM1
0.776 0.160 15 63060899 missense variant G/A snv 1.6E-05 2.8E-05 9
rs1249958
PPP1R1A
0.925 0.040 12 54582053 missense variant C/T snv 2.7E-02 3
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
rs1370940194
KCNA5
12 5044419 missense variant C/T snv 4.4E-06 1
rs71584818
KCNA5
12 5044245 missense variant A/T snv 2.4E-04 2.0E-04 1
rs3745297
HRC
0.790 0.120 19 49154952 missense variant A/C snv 0.41 0.38 10
rs143624519
MAPT
0.724 0.240 17 45991484 missense variant G/A;T snv 1.5E-03; 1.2E-05 17
rs137854606
SCN5A
0.882 0.120 3 38604062 missense variant C/A snv 4
rs45627438
SCN5A
0.925 0.080 3 38604025 missense variant C/T snv 5.8E-05 2.8E-05 3
rs184442491
SCN5A
1.000 0.120 3 38603888 missense variant C/A snv 2.1E-04 7.7E-04 2
rs199473142
SCN5A
1.000 0.120 3 38597952 missense variant C/T snv 2.1E-05 2
rs199473580
SCN5A
1.000 0.120 3 38597926 missense variant G/A snv 1.6E-05 7.0E-06 2
rs137854605
SCN5A
1.000 0.120 3 38581337 missense variant GA/TT mnv 2
rs7626962
SCN5A
0.790 0.080 3 38579416 missense variant G/A;T snv 1.6E-05; 5.9E-03 10
rs137854618
SCN5A
0.742 0.120 3 38566426 missense variant C/A;T snv 8.0E-06 15
rs199473225
SCN5A
0.851 0.120 3 38560397 missense variant G/A;C snv 6
rs199473604
SCN5A
0.882 0.120 3 38560394 missense variant G/T snv 4