Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs6687758 0.763 0.200 1 221991606 regulatory region variant A/G snv 0.20 11
rs11087784 0.776 0.080 20 7760329 intergenic variant A/G snv 0.13 10
rs11190164 0.776 0.080 10 99591947 intergenic variant A/G snv 0.19 10
rs11610543 0.776 0.080 12 42740389 intergenic variant A/G;T snv 10
rs116353863 0.776 0.080 6 31042408 regulatory region variant T/C snv 2.2E-02 10
rs12149163 0.776 0.080 16 86305709 upstream gene variant T/C snv 0.49 10
rs12447408 0.776 0.080 16 86218938 downstream gene variant G/A snv 0.21 10
rs12514517 0.776 0.080 5 40279974 intergenic variant G/A snv 0.21 10
rs12672022 0.776 0.080 7 45096824 downstream gene variant T/C snv 0.13 10
rs12708491 0.776 0.080 15 32700635 downstream gene variant G/A snv 0.33 10
rs13086367 0.776 0.080 3 113185041 downstream gene variant A/G snv 0.38 10
rs13149359 0.776 0.080 4 94017467 intergenic variant C/A snv 0.29 10
rs13204733 0.776 0.080 6 55701310 intergenic variant A/G snv 0.10 10
rs1427760 0.776 0.080 12 114662909 upstream gene variant T/C snv 0.49 10
rs1512436 0.790 0.080 11 106436144 intergenic variant T/C snv 0.50 10
rs16969681 0.776 0.080 15 32700910 downstream gene variant C/T snv 0.11 10
rs17035310 0.790 0.080 4 105143597 upstream gene variant C/T snv 0.14 10
rs17102823 0.776 0.080 14 34894698 intergenic variant A/C;G snv 10
rs189583 0.776 0.080 20 6395810 regulatory region variant G/C;T snv 10
rs1924816 0.776 0.080 13 73423824 intron variant A/G snv 0.29 10
rs2423279 0.790 0.080 20 7831703 downstream gene variant T/C snv 0.29 10
rs28488 0.776 0.080 20 6781574 downstream gene variant C/T snv 0.68 10
rs2965667 0.776 0.080 12 17291799 intergenic variant A/T snv 0.96 10
rs3133285 0.776 0.080 8 116617172 intergenic variant G/C snv 0.19 10
rs34405347 0.776 0.080 9 98917470 regulatory region variant T/C;G snv 10