Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs10069554 5 33204354 intron variant T/C snv 0.45 1
rs10279895 7 27288591 intergenic variant A/G snv 2.9E-02 1
rs10491093 17 10978681 intergenic variant T/G snv 0.72 1
rs10496288 2 83065441 intergenic variant T/C snv 0.13 1
rs10496289 2 83066256 intergenic variant C/T snv 0.13 1
rs10737175 1 159750152 intergenic variant T/C snv 0.24 1
rs11020821 11 94538497 intergenic variant C/A snv 0.28 1
rs1125226 8 58506952 downstream gene variant C/A snv 0.54 1
rs11658572 17 10979696 intergenic variant C/T snv 0.58 1
rs12522034 5 36425491 intergenic variant G/A;C;T snv 1
rs145054295 11 96709521 intron variant AT/- del 7.0E-03 1
rs1468326 12 748335 upstream gene variant A/C;T snv 1
rs16827043 1 146039555 upstream gene variant C/T snv 0.89 1
rs180912 10 113982069 regulatory region variant T/G snv 0.56 1
rs1979255 4 189396926 intergenic variant C/G snv 0.64 1
rs2447182 8 119341744 intergenic variant A/G snv 0.83 1
rs275646 3 148745735 downstream gene variant T/C snv 0.95 1
rs35434 12 115116871 intergenic variant G/A snv 0.22 1
rs35530071 17 7659807 downstream gene variant TT/-;T;TTT;TTTT;TTTTT;TTTTTTTTTTTTT delins 1
rs4267385 17 63506395 intron variant C/T snv 0.61 1
rs4463623 1 188331737 intergenic variant C/T snv 0.29 1
rs4496877 7 150983418 intergenic variant T/G snv 0.74 1
rs4901474 14 54003019 regulatory region variant C/G;T snv 1
rs531003 9 110850339 intergenic variant G/C;T snv 1
rs6677719 1 159753330 intergenic variant C/T snv 0.77 1