Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs763351020 0.633 0.560 7 101132046 missense variant C/T snv 4.0E-06 35
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
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
rs2005108 1.000 0.080 11 102899623 downstream gene variant C/G;T snv 3
rs2295786 1.000 0.080 10 103856724 upstream gene variant A/G;T snv 2
rs2230806 0.689 0.280 9 104858586 missense variant C/T snv 0.32 0.39 24
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
rs880315 0.925 0.120 1 10736809 intron variant T/C snv 0.32 9
rs2228315 0.807 0.120 12 108624122 missense variant C/T snv 0.11 0.14 7
rs599839 0.724 0.360 1 109279544 downstream gene variant G/A;C snv 27
rs147270785 1.000 0.080 1 11046616 missense variant G/A snv 6.5E-04 6.4E-04 2
rs1122608 0.763 0.120 19 11052925 intron variant G/T snv 0.18 16
rs8103309 1.000 0.080 19 11064259 intron variant T/C snv 0.40 2
rs1906591 0.851 0.200 4 110787733 intergenic variant G/A snv 0.15 5
rs2200733 0.752 0.240 4 110789013 intergenic variant C/T snv 0.18 12
rs13143308 0.882 0.120 4 110793263 upstream gene variant T/C;G snv 4
rs6843082 0.925 0.120 4 110796911 non coding transcript exon variant G/A snv 0.71 3
rs10033464 0.807 0.200 4 110799605 downstream gene variant T/G snv 0.86 8
rs3184504 0.572 0.600 12 111446804 missense variant T/A;C;G snv 0.67 92
rs34311906 1.000 0.080 4 112810934 intergenic variant T/C snv 0.43 2
rs7903146 0.554 0.680 10 112998590 intron variant C/G;T snv 93