Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs2643826 3 27521497 upstream gene variant C/T snv 0.56 6
rs35444 12 115114632 intergenic variant A/G snv 0.38 6
rs729302 0.827 0.160 7 128928906 intergenic variant A/C snv 0.28 6
rs7859384 0.882 0.120 9 79507370 intron variant A/C;G snv 6
rs10184428 2 164155317 intron variant C/A;G snv 5
rs1173766 5 32804422 intergenic variant T/C snv 0.57 5
rs16849225 2 164050310 intron variant C/T snv 0.19 5
rs35443 12 115115073 intergenic variant G/C snv 0.40 5
rs4373814 10 18131043 intergenic variant G/C;T snv 5
rs1902859 4 80236549 regulatory region variant T/C snv 0.27 4
rs2770150 0.925 0.080 9 117700861 upstream gene variant A/G snv 0.22 4
rs4459609 0.925 0.120 17 63471587 upstream gene variant C/A snv 0.63 4
rs62524579 8 142979538 downstream gene variant G/A;C;T snv 4
rs743811 0.882 0.160 22 35396981 upstream gene variant T/A;C snv 4
rs864265 0.925 0.080 3 186836503 intergenic variant T/G snv 0.86 4
rs897876 0.882 0.040 2 65564447 intron variant C/T snv 0.30 4
rs112913898 10 103199143 intergenic variant G/A snv 9.1E-02 3
rs11563582 7 27312031 intergenic variant G/A snv 9.8E-02 3
rs12063100 1 188865413 downstream gene variant G/A;T snv 3
rs1463729 0.925 0.120 9 124119169 intergenic variant C/A;T snv 3
rs1656930 1.000 0.080 3 186835068 intergenic variant A/G snv 0.86 3
rs4462906 3 27551369 upstream gene variant T/A;G snv 3
rs6712094 2 164186950 intron variant A/G snv 0.23 3
rs6871087 0.925 0.040 5 30899410 intergenic variant A/G snv 8.5E-02 3
rs7006531 8 94098516 intron variant A/C;G snv 3