Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs751529077 8 17723780 missense variant G/A;T snv 7.7E-05 7.0E-06 1
rs1057518882
CYTB ; ND5 ; ND6
MT 14598 missense variant T/C snv 2
rs104894572 1.000 0.120 17 75765055 missense variant G/A;T snv 8.9E-06 2
rs121909124 1.000 6 42185686 missense variant C/T snv 1.0E-04 3.5E-05 2
rs730882241 1.000 1 230995876 missense variant G/A snv 1.2E-05 2.1E-05 3
rs111699024 0.925 0.120 10 68231485 missense variant T/C;G snv 8.7E-03; 8.8E-06 3
rs539612316 0.925 0.120 2 73449346 stop gained T/A snv 2.0E-05 1.4E-05 4
rs1057518822 1.000 0.080 12 88102888 stop gained G/A snv 4
rs147394623 0.882 0.080 1 26438228 missense variant A/G snv 2.3E-04 1.5E-04 4
rs763544450
ERG
1.000 0.080 21 38445560 missense variant T/G snv 4.0E-06 4
rs1177783734 0.925 0.080 8 18083991 missense variant T/G snv 4.5E-06 7.0E-06 4
rs62636299 0.882 0.040 1 68431371 missense variant C/G snv 4.0E-06 1.4E-05 4
rs62653011 0.882 0.080 1 68438213 missense variant A/G snv 6.8E-05 7.7E-05 4
rs61750654 0.925 0.120 1 94000870 stop gained G/A snv 2.0E-05 7.0E-06 5
rs886043303 0.851 0.200 12 88120121 frameshift variant CTCT/- delins 7.0E-06 5
rs121918632 0.851 0.120 2 165996099 missense variant A/G snv 7.0E-06 5
rs1553348960 0.882 0.080 2 55870851 missense variant A/G snv 5
rs151045328 0.851 0.200 11 17531431 synonymous variant C/T snv 3.6E-05 2.1E-05 5
rs111033272 0.851 0.200 1 216325499 missense variant G/A;T snv 4.0E-06; 2.8E-05 7
rs61750172 0.807 0.080 17 8014700 missense variant C/A;T snv 4.0E-06 8
rs28936700 0.776 0.120 2 38075207 missense variant C/G;T snv 5.0E-06; 3.2E-04 9
rs80358284 0.790 0.240 11 86952443 missense variant T/A;C snv 4.0E-06; 2.4E-05 10
rs104893768
RHO
0.807 0.080 3 129528801 missense variant C/A snv 11
rs142285818
RHO
0.807 0.120 3 129532727 missense variant C/G;T snv 9.7E-04 4.1E-04 11
rs376493409 0.742 0.280 12 88083161 stop gained G/A;T snv 7.0E-05 12