Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs7903146 0.554 0.680 10 112998590 intron variant C/G;T snv 93
rs1260326 0.645 0.600 2 27508073 missense variant T/C;G snv 0.63; 4.0E-06 0.68 81
rs780094 0.658 0.400 2 27518370 intron variant T/C snv 0.67 62
rs12255372 0.667 0.480 10 113049143 intron variant G/A;T snv 28
rs10830963 0.776 0.400 11 92975544 intron variant C/G snv 0.22 27
rs13266634 0.724 0.480 8 117172544 missense variant C/A;T snv 0.29 23
rs174537 0.708 0.400 11 61785208 non coding transcript exon variant G/T snv 0.28 23
rs10811661 0.724 0.400 9 22134095 intergenic variant T/C snv 0.14 22
rs651007 0.851 0.160 9 133278431 upstream gene variant T/A;C snv 22
rs4506565 0.790 0.280 10 112996282 intron variant A/G;T snv 22
rs4402960 0.724 0.400 3 185793899 intron variant G/T snv 0.38 21
rs174535 0.776 0.280 11 61783884 missense variant T/A;C;G snv 0.38 0.32 19
rs560887 0.827 0.120 2 168906638 intron variant T/C snv 0.79 0.80 18
rs174583 0.807 0.320 11 61842278 intron variant C/T snv 0.35 16
rs174576 0.851 0.200 11 61836038 intron variant C/A;T snv 14
rs4841132 8 9326086 non coding transcript exon variant A/G snv 0.89 14
rs174550 0.925 0.160 11 61804006 5 prime UTR variant T/C snv 0.28 13
rs7756992 0.827 0.240 6 20679478 intron variant A/G;T snv 12
rs1387153 0.807 0.200 11 92940662 downstream gene variant C/G;T snv 10
rs2068834 0.925 0.120 2 27616672 intron variant T/C snv 0.28 10
rs11708067 0.882 0.080 3 123346931 intron variant A/G snv 0.19 9
rs2657879 1.000 0.080 12 56471554 missense variant A/G snv 0.17 0.15 9
rs2126259 1.000 8 9327636 intron variant T/C snv 0.87 9
rs1919128 0.882 0.120 2 27578892 missense variant A/G snv 0.30 0.24 8
rs9368222 1.000 0.080 6 20686765 intron variant C/A;T snv 8