Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1022261 4 35474678 intergenic variant A/C snv 0.52 1
rs10252114 7 122315414 upstream gene variant T/C snv 0.37 1
rs10461104 4 27488957 intergenic variant G/A snv 0.68 1
rs10952199 7 1625703 downstream gene variant C/T snv 0.41 1
rs11066971 12 114165055 intergenic variant C/T snv 0.10 1
rs11166986 8 140646056 TF binding site variant G/A;T snv 1
rs11255908 10 8760949 intergenic variant T/G snv 0.35 1
rs1174864 7 53059866 intergenic variant G/A snv 0.52 1
rs117898875 3 84223836 regulatory region variant T/C snv 3.3E-02 1
rs11808210 1 227327348 intergenic variant G/A snv 6.7E-02 1
rs11876432 18 45089460 regulatory region variant C/G snv 0.18 1
rs12030183 1 41295548 intron variant T/C snv 0.28 1
rs12042107 1 90730619 downstream gene variant T/C snv 0.59 1
rs12211126 6 66839558 intergenic variant T/C snv 0.28 1
rs12456711 18 280897 intergenic variant A/G snv 0.22 1
rs1246265 9 84146830 regulatory region variant T/C snv 0.76 1
rs12476173 2 117490138 intergenic variant G/A snv 0.48 1
rs12517438 5 30841947 intergenic variant T/G snv 0.40 1
rs12535004 7 115307058 intergenic variant T/C snv 0.28 1
rs12600773 17 52258612 intergenic variant C/T snv 0.26 1
rs12662631 6 93132728 intergenic variant C/T snv 0.23 1
rs12680810 8 77231908 intergenic variant T/A snv 0.35 1
rs12690535 2 225394657 intergenic variant G/A;C snv 1
rs12825376 12 120742136 intron variant C/T snv 7.2E-02 1
rs12997449 2 178174845 intergenic variant A/G snv 8.2E-02 1