Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1810502 0.790 0.080 20 50440951 intergenic variant C/T snv 0.49 9
rs1871438 0.790 0.080 15 92316651 intron variant A/G snv 0.44 9
rs1886450 0.790 0.080 13 73412491 upstream gene variant A/G snv 0.65 9
rs2189261 0.790 0.080 8 90159507 intergenic variant G/A snv 0.64 9
rs2193352 0.790 0.080 10 99586852 intergenic variant A/G snv 0.15 9
rs2696839 0.790 0.080 16 86306842 intergenic variant G/A;C snv 9
rs2730985 0.790 0.080 12 42736822 intergenic variant A/G snv 0.47 9
rs285245 0.790 0.080 19 16310006 intron variant C/T snv 0.14 9
rs2901879 0.790 0.080 2 66738934 intergenic variant C/T snv 0.54 9
rs35360328 0.790 0.080 3 40883471 intergenic variant T/A snv 0.11 9
rs35509282 0.790 0.080 4 162412253 intergenic variant T/A snv 0.15 9
rs4341754 0.790 0.080 16 80005724 intergenic variant G/C snv 0.44 9
rs4407073 0.790 0.080 16 80022910 intergenic variant T/A;C;G snv 9
rs4954585 0.790 0.080 2 136240824 intergenic variant C/G;T snv 9
rs57046232 0.790 0.080 20 6399697 intergenic variant T/A;C snv 9
rs58791712 0.790 0.080 5 40281696 intergenic variant T/-;TT;TTT delins 9
rs6055286 0.790 0.080 20 7737398 intergenic variant A/G;T snv 9
rs6061231 0.790 0.080 20 62381861 downstream gene variant C/A snv 0.28 9
rs6065668 0.790 0.080 20 43904181 regulatory region variant C/T snv 0.23 9
rs6085661 0.790 0.080 20 6712481 TF binding site variant C/T snv 0.30 9
rs6091213 0.790 0.080 20 50768208 TF binding site variant T/A;C snv 9
rs61336918 0.790 0.080 16 79973369 intergenic variant A/T snv 0.65 9
rs6469656 0.790 0.080 8 116635549 regulatory region variant G/A;C snv 9
rs6658977 0.790 0.080 1 221876478 downstream gene variant G/T snv 0.29 9
rs6691195 0.790 0.080 1 221989031 downstream gene variant C/A snv 0.19 9