Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs4647924 0.600 0.520 4 1801844 missense variant C/A;G;T snv 4.2E-06; 4.2E-06 49
rs1558939623 0.732 0.480 2 174824479 missense variant C/T snv 19
rs72474224 0.708 0.440 13 20189473 missense variant C/A;T snv 7.7E-03 18
rs1553212868 0.807 0.280 1 151406264 frameshift variant G/- delins 17
rs1555741826 0.776 0.280 19 49601646 frameshift variant TGCC/- delins 16
rs1555817157 0.742 0.280 20 25339320 frameshift variant TCTTCCTCAGGCG/- del 16
rs199474657
TRNL1 ; ND1 ; ND2
0.752 0.360 MT 3243 non coding transcript exon variant A/G snv 15
rs1135401743 0.776 0.320 2 42769785 stop gained C/A;T snv 4.0E-06 11
rs80358284 0.790 0.240 11 86952443 missense variant T/A;C snv 4.0E-06; 2.4E-05 10
rs80356529 0.827 0.240 3 193643996 missense variant G/A;C snv 9
rs1057517491 0.776 0.240 13 20189448 frameshift variant C/- delins 8
rs1566304640 0.827 0.280 13 77900593 missense variant G/A snv 8
rs281874674 0.827 0.280 X 108597479 missense variant G/C;T snv 8
rs35887622 0.790 0.200 13 20189481 missense variant A/C;G snv 8.7E-03 8
rs387906930 0.790 0.360 4 6301846 missense variant C/G;T snv 8
rs104894403 0.851 0.240 13 20189386 missense variant C/A;G;T snv 4.0E-06 7
rs72561723 0.790 0.240 13 20189448 missense variant C/T snv 8.0E-06 7
rs104894409 0.827 0.120 13 20189332 missense variant C/A;G;T snv 1.6E-05; 3.6E-05; 4.0E-06 6
rs111033437 0.882 0.120 11 77179925 missense variant G/A;T snv 6
rs1555661648 0.882 0.240 18 26862297 missense variant C/G snv 6
rs1564494285
RET
0.882 0.200 10 43111219 frameshift variant TG/- delins 6
rs185645212 0.851 0.240 15 89323504 missense variant C/A;T snv 8.0E-06; 9.7E-04 6
rs200455852 0.851 0.200 8 18064458 missense variant T/C;G snv 5.8E-05 6
rs28938175 0.851 0.120 14 30877640 missense variant C/T snv 4.0E-06 6
rs587781262 0.882 0.240 X 107640938 missense variant A/G snv 6