Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs10938397 0.851 0.200 4 45180510 intergenic variant A/G snv 0.37 19
rs7138803 0.827 0.240 12 49853685 intergenic variant G/A;T snv 17
rs543874 1.000 0.080 1 177920345 upstream gene variant A/G snv 0.21 11
rs12967135 18 60181790 intergenic variant G/A snv 0.24 8
rs2820443 0.882 0.120 1 219580167 regulatory region variant T/C snv 0.23 8
rs10132280 14 25458973 intergenic variant C/A snv 0.37 6
rs17391694 0.882 0.120 1 78157942 regulatory region variant C/T snv 7.8E-02 6
rs887912 1.000 0.080 2 59075742 intron variant T/C;G snv 6
rs12936587 0.882 0.080 17 17640408 regulatory region variant G/A snv 0.38 5
rs11152213 1.000 0.080 18 60185715 intergenic variant A/C;T snv 4
rs62104180 2 466003 intergenic variant G/A snv 2.9E-02 4
rs663129 0.882 0.160 18 60171168 intergenic variant G/A snv 0.24 4
rs10929925 2 6015425 intergenic variant C/A;T snv 3
rs11863065 16 82293200 intergenic variant G/A snv 7.3E-02 3
rs59992789 18 60346332 intron variant T/C snv 0.18 3
rs6755502 2 635721 intergenic variant T/C snv 0.85 3
rs11165623 1 96427444 intergenic variant G/A;T snv 2
rs11607976 11 69464343 upstream gene variant C/G;T snv 2
rs11873305 1.000 0.080 18 60381959 intron variant A/C snv 0.12 2
rs1320330 2 622225 intergenic variant T/A;G snv 2
rs146144484 6 3865792 intron variant C/G;T snv 2
rs34898535 16 31014320 upstream gene variant C/A;G;T snv 2
rs397778224 16 19912366 regulatory region variant -/C delins 0.21 2
rs532504 1 177909798 intron variant G/A snv 0.17 2
rs6751993 2 635864 intergenic variant A/G snv 0.85 2