Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1027009063 0.925 0.040 2 8802974 stop gained G/A snv 2
rs10404453 1.000 0.040 19 51693235 non coding transcript exon variant G/A;C snv 2.6E-03; 5.5E-06 1
rs1041163 0.882 0.160 1 100718269 upstream gene variant T/C snv 0.18 3
rs1050501 0.732 0.440 1 161674008 missense variant T/C snv 0.16 0.19 15
rs1058885 0.925 0.080 1 109923844 missense variant T/C snv 0.38 0.39 2
rs11112872 1.000 0.040 12 106111556 intron variant T/G snv 0.28 1
rs11225395 0.776 0.360 11 102725749 intron variant A/C;G snv 11
rs113420705 0.925 0.160 4 184649399 5 prime UTR variant T/C snv 0.31 4
rs11362 0.742 0.360 8 6877877 5 prime UTR variant C/T snv 0.43 0.40 13
rs1143627 0.605 0.760 2 112836810 5 prime UTR variant G/A snv 0.56 47
rs1143634 0.597 0.680 2 112832813 synonymous variant G/A snv 0.19 0.19 52
rs11614913 0.512 0.760 12 53991815 mature miRNA variant C/T snv 0.39 0.34 111
rs1171989978 1.000 0.040 1 202159420 missense variant G/A snv 4.0E-06 1
rs11747270 0.790 0.240 5 150879305 intron variant A/G snv 0.21 7
rs12449783 1.000 0.040 17 30200635 intron variant A/C;T snv 1
rs12976445 0.689 0.600 19 51693200 non coding transcript exon variant T/C snv 0.45 20
rs12979860 0.547 0.520 19 39248147 intron variant C/T snv 0.39 84
rs1333048 0.683 0.320 9 22125348 intron variant A/C snv 0.44 24
rs1342913 0.851 0.040 1 190151895 intron variant G/A snv 0.61 4
rs1416580204
MOK
0.608 0.720 14 102250837 missense variant C/T snv 4.0E-06 7.0E-06 49
rs148704956 0.716 0.360 6 52187772 missense variant A/G snv 8.0E-06 7.0E-06 19
rs1595009 1.000 0.040 4 73968939 intergenic variant C/T snv 0.61 1
rs16944 0.531 0.920 2 112837290 upstream gene variant A/G snv 0.57 92
rs1799750 0.592 0.760 11 102799765 intron variant C/- delins 0.50 48
rs1799964 0.608 0.760 6 31574531 upstream gene variant T/C snv 0.19 47