Source: CURATED

Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs10510126 1.000 0.080 10 123242969 regulatory region variant C/T snv 0.12 1
rs1079866 0.925 0.080 7 41430495 intergenic variant C/G snv 0.13 1
rs11668840 1.000 0.080 19 17288816 upstream gene variant T/C snv 0.47 1
rs12118297 0.925 0.080 1 87313534 intergenic variant G/T snv 0.19 1
rs12285889 1.000 0.080 11 97291056 intergenic variant A/G snv 0.17 1
rs12974508 1.000 0.080 19 17290712 upstream gene variant C/A;T snv 0.47 1
rs12975707 1.000 0.080 19 17290871 upstream gene variant A/G snv 0.33 1
rs13188458 0.882 0.160 5 8127718 intergenic variant T/G snv 0.22 1
rs140068132 0.925 0.080 6 151633699 TF binding site variant A/G snv 1.1E-02 1
rs1586840 1.000 0.080 12 19909563 intron variant G/A snv 0.96 1
rs16886034 0.925 0.080 5 56688029 intergenic variant T/C;G snv 5.4E-02 1
rs16886113 0.925 0.080 5 56699208 intergenic variant T/G snv 8.3E-02 1
rs16886181 0.925 0.080 5 56733416 regulatory region variant T/C snv 0.17 1
rs17094222 0.925 0.080 10 100635683 intergenic variant T/C snv 0.17 1
rs17136641 1.000 0.080 11 69513744 intergenic variant G/A snv 0.16 1
rs17529111 0.925 0.080 6 81418669 intergenic variant T/C snv 0.18 1
rs199860 1.000 0.080 X 38883510 intergenic variant T/C snv 0.41 1
rs2184380 1.000 0.080 10 8672111 intergenic variant G/C;T snv 1
rs2198600 1.000 0.080 12 54746618 intergenic variant C/T snv 0.52 1
rs2364542 1.000 0.080 19 17346743 downstream gene variant G/A snv 0.31 1
rs2494251 0.925 0.080 1 159311361 downstream gene variant G/A;C snv 1
rs2736108 0.807 0.160 5 1297373 upstream gene variant C/T snv 0.24 1
rs34963425 1.000 0.080 19 17247380 intron variant C/A;T snv 1
rs35630819 1.000 0.080 19 17248490 intron variant C/T snv 6.4E-02 1
rs3857481 1.000 0.080 6 86414851 intergenic variant G/A snv 0.29 1