Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs10895068 0.752 0.240 11 101129483 5 prime UTR variant C/T snv 3.6E-02 14
rs763351020 0.633 0.560 7 101132046 missense variant C/T snv 4.0E-06 35
rs2228611 0.708 0.520 19 10156401 synonymous variant T/A;C snv 0.52 19
rs1416580204
MOK
0.608 0.720 14 102250837 missense variant C/T snv 4.0E-06 7.0E-06 49
rs6214 0.672 0.400 12 102399791 3 prime UTR variant C/T snv 0.45 26
rs5498 0.531 0.760 19 10285007 missense variant A/G snv 0.44 0.37 99
rs4684677 0.742 0.360 3 10286769 missense variant T/A snv 0.10 6.6E-02 13
rs2075356 0.882 0.160 3 10287125 non coding transcript exon variant T/C snv 8.3E-02 5
rs861539 0.519 0.680 14 103699416 missense variant G/A snv 0.29 0.30 104
rs1805097 0.689 0.360 13 109782884 missense variant C/G;T snv 0.35 22
rs1143623 0.677 0.440 2 112838252 upstream gene variant C/G snv 0.24 29
rs7903146 0.554 0.680 10 112998590 intron variant C/G;T snv 93
rs12255372 0.667 0.480 10 113049143 intron variant G/A;T snv 28
rs1800497 0.620 0.400 11 113400106 missense variant G/A snv 0.26 0.26 56
rs670 0.763 0.360 11 116837697 5 prime UTR variant C/T snv 0.17 13
rs397507444 0.405 0.880 1 11794407 missense variant T/G snv 306
rs1217691063 0.330 0.920 1 11796309 missense variant A/G snv 4.0E-06 7.0E-06 614
rs1801133 0.472 0.880 1 11796321 missense variant G/A snv 0.31 0.27 174
rs7566605 0.752 0.320 2 118078449 regulatory region variant C/G snv 0.70 11
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
rs3856806 0.637 0.440 3 12434058 synonymous variant C/T snv 0.13 0.11 41
rs7799039 0.649 0.560 7 128238730 upstream gene variant G/A;C snv 33
rs895819 0.623 0.560 19 13836478 non coding transcript exon variant T/A;C;G snv 0.34 0.38 46
rs1042713 0.576 0.800 5 148826877 missense variant G/A snv 0.42 0.43 63