Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs867410737 0.708 0.440 19 1242559 missense variant C/T snv 6.7E-06 42
rs386134243 0.708 0.360 1 156135967 missense variant C/A;T snv 4.0E-06 16
rs766265889 0.827 0.240 2 178535508 stop gained G/A;T snv 8.0E-06; 4.0E-06 11
rs114638163 0.827 0.240 13 23805994 stop gained C/A;T snv 4.0E-06; 1.3E-03 10
rs140614802 0.851 0.040 14 104741231 missense variant G/A snv 3.4E-05 2.8E-05 10
rs45546039 0.732 0.120 3 38613781 missense variant C/A;T snv 4.1E-06 10
rs397516955
DSP
0.790 0.120 6 7562753 stop gained G/A snv 9
rs111033560 0.807 0.040 6 118559037 stop gained T/G snv 1.6E-05 7
rs574660186 0.807 0.200 2 178579702 stop gained G/A;C snv 1.6E-05 3.5E-05 7
rs760187215 1.000 0.040 14 23431859 missense variant C/T snv 8.0E-06 6
rs137854618 0.742 0.120 3 38566426 missense variant C/A;T snv 8.0E-06 5
rs397516248 0.851 0.200 14 23415153 missense variant C/T snv 5
rs397517689 0.882 0.160 2 178574530 stop gained G/A snv 4.0E-06 5
rs45586240 0.827 0.080 1 201361989 missense variant G/A;T snv 4.0E-06 5
rs606231324 0.851 0.080 14 23428505 missense variant C/G;T snv 5
rs727503204 0.882 0.080 11 47343020 splice donor variant C/G;T snv 5
rs727504443
DSP
0.851 0.120 6 7565521 splice donor variant G/A snv 7.0E-06 5
rs74315379 0.827 0.080 1 201364336 missense variant G/A;T snv 1.2E-04 5
rs1114167453 1.000 19 45385569 stop gained G/C snv 4
rs143139258 0.882 0.080 12 110913097 missense variant T/G snv 2.0E-04 2.9E-04 4
rs1553265736 0.925 0.040 1 156136080 missense variant G/C snv 4
rs1554093433 0.925 0.080 5 173232833 stop gained G/T snv 4
rs1554108012
DSP
0.882 0.120 6 7579323 stop gained C/T snv 4
rs1554108431
DSP
0.882 0.120 6 7581189 stop gained C/T snv 4
rs1557315928
DMD
X 32380517 stop gained C/T snv 4