Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs104886003 0.562 0.440 3 179218303 missense variant G/A;C snv 4.0E-06 71
rs17655 0.597 0.560 13 102875652 missense variant G/C snv 0.28 0.30 52
rs121913499 0.605 0.520 2 208248389 missense variant G/A;C;T snv 51
rs56149945 0.595 0.680 5 143399752 missense variant T/A;C snv 2.0E-02 49
rs28934578 0.605 0.600 17 7675088 missense variant C/A;T snv 4.0E-06 47
rs121912664 0.630 0.320 17 7670699 missense variant C/A;G;T snv 1.2E-05 44
rs79184941 0.617 0.600 10 121520163 missense variant G/A;C snv 5.6E-05; 4.0E-06 41
rs5370 0.630 0.520 6 12296022 missense variant G/T snv 0.23 0.21 37
rs752742313 0.637 0.320 3 138655502 missense variant C/T snv 1.2E-05 36
rs1136201 0.645 0.280 17 39723335 missense variant A/G;T snv 0.20 34
rs1800449
LOX
0.641 0.400 5 122077513 missense variant C/A;T snv 4.0E-06; 0.17 33
rs368087026 0.637 0.520 21 45530890 missense variant G/A snv 33
rs1058808 0.658 0.360 17 39727784 missense variant C/G snv 0.61 0.52 27
rs11556218 0.653 0.600 15 81305928 missense variant T/G snv 9.6E-02 0.12 27
rs764146326 0.662 0.480 17 7673779 missense variant C/A;G;T snv 4.0E-06 25
rs747342068 0.695 0.440 17 7675218 missense variant T/C;G snv 4.0E-06 21
rs1273593548 0.716 0.160 7 106867593 missense variant T/G snv 8.4E-06 19
rs199476133
ND3 ; COX3 ; ND4L ; ND4 ; ATP8 ; ATP6
0.742 0.320 MT 8993 missense variant T/C;G snv 18
rs747126003 0.689 0.400 7 22728790 missense variant A/G;T snv 4.0E-06 18
rs4072111 0.716 0.400 15 81285798 missense variant C/T snv 0.17 0.11 16
rs1057519736 0.752 0.160 15 90088605 missense variant C/G snv 13
rs367597251 0.807 0.080 12 68839587 missense variant A/G snv 1.5E-04 5.1E-04 10
rs235768 0.807 0.160 20 6778468 missense variant A/G;T snv 0.67 8
rs56307747 0.776 0.160 7 74059952 missense variant G/A;C snv 4.0E-06 8
rs3745406 0.851 0.080 19 53891711 missense variant T/A;C snv 4.0E-06; 0.41 6