Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1801253 0.683 0.440 10 114045297 missense variant G/C snv 0.74 0.69 34
rs174547 0.742 0.240 11 61803311 intron variant T/C snv 0.28 33
rs10401969 0.776 0.240 19 19296909 intron variant T/C snv 0.10 25
rs1333048 0.683 0.320 9 22125348 intron variant A/C snv 0.44 24
rs4803750 0.807 0.240 19 44744370 upstream gene variant A/G snv 7.7E-02 22
rs2383207 0.695 0.280 9 22115960 intron variant A/G snv 0.64 22
rs629301 0.851 0.120 1 109275684 3 prime UTR variant G/T snv 0.74 22
rs375752214 0.708 0.400 7 150998541 missense variant C/T snv 4.1E-06 4.2E-05 22
rs4506565 0.790 0.280 10 112996282 intron variant A/G;T snv 22
rs562338 0.807 0.160 2 21065449 intergenic variant A/G snv 0.69 21
rs247617 0.827 0.160 16 56956804 regulatory region variant C/A snv 0.29 20
rs261332 0.851 0.120 15 58435126 non coding transcript exon variant A/G snv 0.80 20
rs2074755 0.807 0.240 7 73462836 non coding transcript exon variant T/C snv 9.2E-02 20
rs2108622 0.742 0.280 19 15879621 missense variant C/T snv 0.27 0.22 20
rs12976445 0.689 0.600 19 51693200 non coding transcript exon variant T/C snv 0.45 20
rs1728918 0.827 0.160 2 27412596 upstream gene variant A/G;T snv 19
rs12579302 0.851 0.120 12 89656726 intron variant A/G snv 0.15 19
rs478442 0.851 0.120 2 21176344 intergenic variant G/C;T snv 18
rs765547 0.827 0.160 8 20008763 intergenic variant G/A;C;T snv 18
rs7703051 0.851 0.120 5 75329662 intron variant C/A snv 0.38 18
rs4244285 0.695 0.360 10 94781859 synonymous variant G/A;C snv 0.18 18
rs1805123 0.724 0.280 7 150948446 missense variant T/A;C;G snv 1.3E-05; 0.18; 8.4E-06 18
rs5744680 0.851 0.120 5 75584065 intron variant G/A snv 0.55 18
rs799165 0.851 0.120 7 73637727 intergenic variant T/A snv 0.13 17
rs1801252 0.724 0.320 10 114044277 missense variant A/G snv 0.15 0.17 17