Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs143282828 1.000 0.080 5 176968697 missense variant A/G snv 7.3E-04 7.3E-04 1
rs144567652 0.776 0.200 14 45198718 stop gained C/A;T snv 4.0E-06; 1.0E-03 8
rs147120792 0.851 0.200 13 49630839 missense variant C/A;T snv 3.0E-02 6
rs152451 1.000 0.080 16 23634870 missense variant T/A;C snv 0.10 1
rs16940 0.882 0.080 17 43093220 synonymous variant A/G snv 0.35 0.29 5
rs1695 0.457 0.880 11 67585218 missense variant A/G snv 0.34 0.36 188
rs17663555 1.000 0.080 5 73136209 intron variant C/A;G;T snv 3
rs1799782 0.474 0.800 19 43553422 missense variant G/A snv 9.5E-02 7.0E-02 151
rs1801132 0.689 0.320 6 151944387 synonymous variant G/C snv 0.73 0.80 22
rs1801201 1.000 0.080 17 39723332 missense variant A/C;G snv 4.0E-06; 4.9E-03 1
rs203462 0.807 0.200 17 19909228 missense variant T/C snv 0.37 0.43 7
rs2046210 0.708 0.280 6 151627231 intergenic variant G/A snv 0.41 21
rs2070094 0.882 0.080 2 214767531 missense variant C/A;T snv 1.6E-05; 0.37 3
rs2241268 1.000 0.080 15 85735078 missense variant G/A snv 0.22 0.19 1
rs2420946 0.851 0.160 10 121591810 intron variant T/C snv 0.56 4
rs25487 0.441 0.800 19 43551574 missense variant T/C snv 0.68 0.71 205
rs28359178
CYTB ; ND5 ; ND6
0.882 0.280 MT 13708 missense variant G/A snv 3
rs28363284 0.882 0.080 17 35103294 missense variant T/C snv 9.7E-03 1.1E-02 5
rs28904921 0.763 0.320 11 108329202 missense variant T/G snv 4.0E-05 6.3E-05 12
rs28997576 0.776 0.160 2 214752454 missense variant C/G;T snv 1.5E-02 11
rs2981582 0.695 0.360 10 121592803 intron variant A/G snv 0.58 21
rs3112612 0.882 0.080 16 52601252 intron variant G/A snv 0.44 3
rs3218536 0.620 0.440 7 152648922 missense variant C/G;T snv 4.0E-06; 6.4E-02 37
rs34301344 0.689 0.400 13 49630893 stop gained G/A snv 9.7E-03 7.9E-03 22
rs34434221 0.882 0.080 15 85579644 missense variant A/C snv 2.2E-02 2.2E-02 3