Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs13392272 2 20994618 downstream gene variant C/T snv 0.37 5
rs1501908 1.000 0.040 5 156971158 intergenic variant G/A;C;T snv 5
rs4564803 2 20982630 intergenic variant G/T snv 0.25 5
rs509728 11 116662450 downstream gene variant G/C snv 2.7E-02 5
rs56156922 16 56953457 intergenic variant T/C snv 0.26 5
rs675504 11 102959002 upstream gene variant A/G snv 0.98 5
rs10054063 5 173965395 downstream gene variant A/T snv 0.26 4
rs10156121 7 142672656 downstream gene variant T/C snv 3.9E-02 4
rs1016988 5 132408882 upstream gene variant T/C snv 0.20 4
rs1250229 1.000 0.040 2 215439661 upstream gene variant T/C snv 0.77 4
rs16860926 3 186609982 intron variant T/C snv 2.6E-02 4
rs176813 4 68733813 regulatory region variant T/C snv 0.38 4
rs2207132 20 40513876 intergenic variant G/A snv 2.7E-02 4
rs2523575 6 31361049 upstream gene variant C/G snv 0.20 4
rs2954022 8 125470379 intron variant C/A;T snv 4
rs4850047 2 3587163 regulatory region variant T/C snv 0.84 4
rs4870941 8 125486586 intron variant G/C snv 0.20 4
rs5014650 6 160678471 upstream gene variant G/A snv 0.16 4
rs506585 2 21174310 intergenic variant G/A;C;T snv 4
rs563290 2 21065354 intergenic variant G/A snv 0.69 4
rs585362 1 109247173 upstream gene variant C/G;T snv 4
rs585967 1.000 0.040 2 21047682 upstream gene variant A/C snv 0.81 4
rs5942937 X 110473179 intron variant T/G snv 0.47 4
rs5985471 X 110460733 downstream gene variant C/T snv 0.43 4
rs668948 1.000 0.040 2 21068657 regulatory region variant G/A snv 0.71 4