Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs10127775 1 230160042 intron variant A/G;T snv 4
rs10889332 1.000 0.120 1 62485187 3 prime UTR variant C/T snv 0.39 4
rs12040333 1.000 0.080 1 43848369 intron variant G/A;C snv 2
rs1998013 1 55492357 intron variant C/T snv 4.4E-03 1
rs2390582 1 90478350 intergenic variant A/G snv 0.15 1
rs1260326 0.645 0.600 2 27508073 missense variant T/C;G snv 0.63; 4.0E-06 0.68 81
rs560887 0.827 0.120 2 168906638 intron variant T/C snv 0.79 0.80 18
rs673548 0.925 0.120 2 21014672 intron variant G/A;T snv 14
rs10211524 2 64980940 intron variant G/A snv 0.51 4
rs113533135 1.000 0.080 2 140268867 intron variant T/C snv 2.0E-02 2
rs1532002 1.000 0.080 2 140292500 intron variant G/A snv 2.3E-02 2
rs2680830 1.000 0.080 2 17596817 intron variant A/G;T snv 0.94 2
rs6754498 1.000 0.080 2 185953121 non coding transcript exon variant A/C;G;T snv 2
rs9973676 1.000 0.080 2 230954091 intron variant G/A snv 5.8E-02 2
rs749924 2 242084344 upstream gene variant C/T snv 0.25 1
rs72928364 1.000 0.080 3 100894935 intron variant C/T snv 0.39 2
rs17404667 3 64288876 intron variant C/G snv 6.2E-02 1
rs741013 3 64306961 intron variant A/T snv 6.0E-02 1
rs1440581 1.000 0.080 4 88305270 intron variant T/A;C snv 4
rs1912826 4 186228386 intron variant G/A;C snv 4
rs16850360 4 74006728 intron variant A/G snv 4.2E-02 2
rs7442201 1.000 0.080 4 4360022 intron variant A/C;G snv 2
rs74570061 1.000 0.080 4 56517605 intron variant T/C snv 3.9E-02 2
rs76294234 1.000 0.080 4 83241025 intron variant A/G snv 1.5E-02 2
rs7689240 1.000 0.080 4 35313869 intergenic variant A/G snv 0.21 2