Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs10123021 9 100689786 regulatory region variant G/A;T snv 1
rs3783613 0.851 0.200 1 100731231 missense variant G/A;C snv 4.0E-06; 9.9E-03 6
rs763351020 0.633 0.560 7 101132046 missense variant C/T snv 4.0E-06 35
rs28935197 0.776 0.280 X 101398942 missense variant T/C snv 5.5E-06 10
rs104894845 0.807 0.160 X 101401752 missense variant C/G;T snv 5.5E-04 8
rs11053646 0.724 0.280 12 10160849 missense variant C/G snv 0.11 0.13 18
rs1416580204
MOK
0.608 0.720 14 102250837 missense variant C/T snv 4.0E-06 7.0E-06 49
rs13114738 0.851 0.120 4 102363708 intron variant C/A;T snv 16
rs7136446 0.882 0.160 12 102444737 intron variant C/T snv 0.66 8
rs5498 0.531 0.760 19 10285007 missense variant A/G snv 0.44 0.37 99
rs572527200 0.882 0.240 11 102875064 upstream gene variant T/C snv 4
rs17655 0.597 0.560 13 102875652 missense variant G/C snv 0.28 0.30 52
rs2005108 1.000 0.080 11 102899623 downstream gene variant C/G;T snv 3
rs2986017 0.851 0.120 10 103458495 missense variant A/G snv 0.79 0.80 6
rs2295786 1.000 0.080 10 103856724 upstream gene variant A/G;T snv 2
rs3809021 0.882 0.080 11 104164894 upstream gene variant T/G snv 0.61 4
rs4925 0.677 0.560 10 104263031 missense variant C/A snv 0.25 0.23 28
rs146292819 0.790 0.240 9 104794495 missense variant T/G snv 2.9E-04 3.8E-04 9
rs2066718 0.882 0.120 9 104826974 missense variant C/G;T snv 4.3E-04; 5.4E-02 7
rs2230806 0.689 0.280 9 104858586 missense variant C/T snv 0.32 0.39 24
rs2288904 0.807 0.240 19 10631494 missense variant A/G snv 0.80 0.83 8
rs9797861 0.790 0.200 19 10632450 intron variant C/A;G;T snv 9
rs783396 1.000 0.080 6 106539495 missense variant A/C snv 0.93 0.93 2
rs2229383 1.000 0.080 19 10683954 synonymous variant G/A;C;T snv 4.0E-06; 0.68 2
rs2507800 1.000 0.040 8 107250441 3 prime UTR variant T/A snv 0.36 2