Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1672908 1 52875213 intron variant A/G snv 0.49 1
rs11245450 10 124969506 intron variant G/A snv 0.35 2
rs5762813 22 28807326 intron variant C/T snv 0.25 3
rs4835265 4 145900258 intron variant C/A snv 0.15 5
rs10957985 8 80877686 upstream gene variant G/A snv 0.35 1
rs2732480 12 48342520 3 prime UTR variant C/A snv 0.39 3
rs4801582 19 58402077 intron variant T/G snv 0.66 1
rs78170284 2 27612215 intron variant G/A snv 0.17 1
rs35699219 9 106882096 intron variant A/G snv 0.18 1
rs7259317 19 21510326 intron variant G/T snv 0.61 1
rs12730651 1 33289932 intron variant A/G snv 0.22 1
rs6073972 20 45961659 non coding transcript exon variant C/G snv 0.13 2
rs146207734 17 16569536 upstream gene variant A/G;T snv 1
rs151305716 20 53605567 intron variant C/T snv 8.1E-03 3
rs3801034 7 6694510 intron variant T/C;G snv 1
rs61071861 15 42418021 intron variant G/C snv 0.36 1
rs1050338 7 44768624 3 prime UTR variant G/A snv 0.39 1
rs11002791 10 79040561 intron variant G/A snv 0.37 1
rs67372909 10 79045259 intron variant T/C snv 0.22 1
rs142529006 7 100022093 intron variant T/A snv 6.9E-03 4
rs1007934 14 72996771 intron variant G/A snv 0.33 3
rs6993770 0.925 0.080 8 105569300 intron variant A/T snv 0.31 7
rs74035509 16 88500925 intron variant C/T snv 0.10 5
rs12232460 16 88499645 intron variant G/A;T snv 1
rs4495442 8 143251666 intron variant T/C;G snv 1