Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs28936379 0.807 0.120 1 226888977 missense variant A/C;G;T snv 4.0E-06 10
rs1169288 0.776 0.160 12 120978847 missense variant A/C;T snv 0.35 21
rs1217691063 0.330 0.920 1 11796309 missense variant A/G snv 4.0E-06 7.0E-06 614
rs1137101 0.554 0.760 1 65592830 missense variant A/G snv 0.51 0.50 77
rs4994 0.578 0.640 8 37966280 missense variant A/G snv 0.11 9.2E-02 65
rs1137100 0.627 0.640 1 65570758 missense variant A/G snv 0.30 0.25 39
rs199474657
TRNL1 ; ND1 ; ND2
0.752 0.360 MT 3243 non coding transcript exon variant A/G snv 15
rs744373 0.851 0.160 2 127137039 downstream gene variant A/G snv 0.35 8
rs886205 0.827 0.360 12 111766623 intron variant A/G snv 0.35 8
rs3818361
CR1
0.851 0.080 1 207611623 intron variant A/G snv 0.74 6
rs2297627 0.925 0.120 13 40659794 intron variant A/G snv 0.41 3
rs17446593 1.000 0.080 13 40553948 intron variant A/G snv 0.19 2
rs495490 1.000 0.080 9 22010413 intron variant A/G snv 6.8E-02 2
rs1486559930 11 49175866 missense variant A/G snv 4.0E-06 1
rs63750526 0.776 0.160 14 73192832 missense variant C/A snv 10
rs1799999 0.882 0.160 7 113878379 missense variant C/A snv 0.22 0.17 4
rs13266634 0.724 0.480 8 117172544 missense variant C/A;T snv 0.29 23
rs121909244 0.776 0.160 3 12434111 missense variant C/A;T snv 4.0E-06 11
rs13283456 0.925 0.080 9 128122474 missense variant C/A;T snv 4.0E-06; 0.13 3
rs1801282 0.500 0.840 3 12351626 missense variant C/G snv 0.11 8.9E-02 131
rs1805192 0.510 0.840 3 12379739 missense variant C/G snv 121
rs10830963 0.776 0.400 11 92975544 intron variant C/G snv 0.22 27
rs1799945 0.452 0.760 6 26090951 missense variant C/G;T snv 0.11 0.10 226
rs7903146 0.554 0.680 10 112998590 intron variant C/G;T snv 93
rs1801278 0.637 0.560 2 226795828 missense variant C/G;T snv 4.0E-06; 5.2E-02 38