Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1800896 0.507 0.800 1 206773552 intron variant T/C snv 0.41 113
rs578776 0.742 0.240 15 78596058 3 prime UTR variant G/A snv 0.39 13
rs2240308 0.701 0.360 17 65558473 missense variant G/A snv 0.47 0.39 18
rs9344 0.653 0.480 11 69648142 splice region variant G/A snv 0.45 0.39 34
rs1695 0.457 0.880 11 67585218 missense variant A/G snv 0.34 0.36 188
rs2243250
IL4
0.570 0.760 5 132673462 upstream gene variant C/T snv 0.35 61
rs11614913 0.512 0.760 12 53991815 mature miRNA variant C/T snv 0.39 0.34 111
rs927068 0.925 0.040 20 49561437 intron variant G/T snv 0.32 2
rs2274223 0.620 0.400 10 94306584 missense variant A/G snv 0.28 0.31 40
rs1979277 0.620 0.560 17 18328782 missense variant G/A snv 0.27 0.31 45
rs10484761 0.807 0.080 6 40834522 intergenic variant T/C snv 0.31 7
rs17655 0.597 0.560 13 102875652 missense variant G/C snv 0.28 0.30 52
rs861539 0.519 0.680 14 103699416 missense variant G/A snv 0.29 0.30 104
rs4804217 1.000 0.040 19 7634461 intron variant C/T snv 0.29 3
rs1051740 0.592 0.760 1 225831932 missense variant T/C snv 0.32 0.27 56
rs4919510 0.641 0.520 10 100975021 mature miRNA variant C/G snv 0.27 0.27 32
rs2233406 0.732 0.440 14 35405593 upstream gene variant G/A snv 0.26 12
rs351855 0.597 0.560 5 177093242 missense variant G/A snv 0.33 0.26 58
rs6125671 0.925 0.040 20 49559061 intron variant C/T snv 0.24 2
rs16969968 0.653 0.360 15 78590583 missense variant G/A snv 0.26 0.24 37
rs1052133 0.476 0.800 3 9757089 missense variant C/G snv 0.27 0.22 147
rs2228000
XPC
0.585 0.560 3 14158387 missense variant G/A snv 0.24 0.21 53
rs6019902 0.925 0.040 20 49561676 intron variant G/A snv 0.21 2
rs3746444 0.514 0.760 20 34990448 mature miRNA variant A/G snv 0.20 0.19 105
rs17222691 0.925 0.040 17 58693735 3 prime UTR variant C/T snv 0.17 2