Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs3851179 0.752 0.280 11 86157598 downstream gene variant T/C snv 0.70 15
rs744373 0.851 0.160 2 127137039 downstream gene variant A/G snv 0.35 8
rs3813929 0.851 0.240 X 114584047 upstream gene variant C/G;T snv 5
rs1049673 0.807 0.160 7 80677034 3 prime UTR variant C/G;T snv 7
rs3856806 0.637 0.440 3 12434058 synonymous variant C/T snv 0.13 0.11 41
rs2073162 1.000 0.080 X 100594020 synonymous variant G/A snv 0.40 0.39 2
rs760555162 1.000 0.080 12 6537178 synonymous variant G/A snv 4.0E-06 2
rs775018856 1.000 0.080 17 7283304 synonymous variant G/A snv 2.8E-05 1.4E-05 2
rs199474657
TRNL1 ; ND1 ; ND2
0.752 0.360 MT 3243 non coding transcript exon variant A/G snv 15
rs1884614 0.882 0.080 20 44351879 non coding transcript exon variant C/T snv 0.18 5
rs2293855 0.851 0.120 8 11319901 non coding transcript exon variant G/A snv 0.35 5
rs1217691063 0.330 0.920 1 11796309 missense variant A/G snv 4.0E-06 7.0E-06 614
rs6265 0.436 0.760 11 27658369 missense variant C/T snv 0.19 0.15 272
rs1800562 0.435 0.880 6 26092913 missense variant G/A snv 3.3E-02 3.8E-02 262
rs4680 0.442 0.920 22 19963748 missense variant G/A snv 0.46 0.44 249
rs1799983 0.430 0.880 7 150999023 missense variant T/A;G snv 0.75 246
rs1799945 0.452 0.760 6 26090951 missense variant C/G;T snv 0.11 0.10 226
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
rs1229984 0.570 0.560 4 99318162 missense variant T/C;G snv 0.90 83
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
rs121912438 0.605 0.520 21 31667299 missense variant G/A;C;T snv 1.2E-05; 8.0E-06 58
rs1232898090 0.637 0.600 22 46198429 missense variant G/C;T snv 4.0E-06; 4.0E-06 40
rs1137100 0.627 0.640 1 65570758 missense variant A/G snv 0.30 0.25 39