Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs10037743 5 33163672 intron variant T/C;G snv 1
rs10061757 5 56790978 intergenic variant G/C snv 0.50 1
rs1006660 15 89340289 downstream gene variant T/A;C snv 1
rs1007358 7 46161757 intergenic variant A/G snv 0.23 1
rs1009404 6 113405402 intergenic variant T/C snv 0.71 1
rs10100085 8 40198735 regulatory region variant C/A;G snv 1
rs10121511 9 96626342 intergenic variant A/C;T snv 1
rs10121673 9 108469029 regulatory region variant C/T snv 0.32 1
rs10129429 14 91964487 downstream gene variant G/A;C snv 1
rs10146757 14 95073400 intergenic variant A/G;T snv 1
rs10155941 7 134737981 upstream gene variant T/C snv 0.43 1
rs10179158 2 65784898 intron variant T/C;G snv 1
rs10185143 2 24927889 intergenic variant T/C;G snv 0.57 1
rs10185917 2 171508843 intergenic variant A/G;T snv 1
rs10188078 2 113694652 intron variant G/A snv 0.15 1
rs10203731 2 25678644 upstream gene variant C/G;T snv 1
rs10208141 2 6258395 non coding transcript exon variant T/C snv 0.66 1
rs10253161 7 46956794 intron variant A/G snv 0.32 1
rs10271999 7 27469589 intergenic variant G/A snv 0.44 1
rs1039440 5 51204794 intergenic variant A/G snv 0.48 1
rs10403206 19 46464655 downstream gene variant T/C snv 0.98 1
rs10405035 19 15337087 upstream gene variant G/A snv 0.55 1
rs10435093 7 25246386 intergenic variant A/T snv 0.22 1
rs10456943 6 121556819 regulatory region variant A/C snv 0.11 1
rs10460436 2 231950631 intergenic variant G/A snv 5.7E-02 1