Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs2943650 0.827 0.120 2 226241205 intergenic variant C/T snv 0.58 6
rs29941 1.000 0.080 19 33818627 downstream gene variant A/G snv 0.70 6
rs4854344 1.000 0.080 2 638144 regulatory region variant G/T snv 0.82 6
rs8089364 0.925 0.120 18 60191596 upstream gene variant T/C snv 0.21 6
rs887912 1.000 0.080 2 59075742 intron variant T/C;G snv 6
rs979012 1.000 0.080 20 6642727 intergenic variant T/C snv 0.67 6
rs11977021 0.827 0.240 7 106288069 upstream gene variant C/T snv 0.22 5
rs2197089 0.925 0.080 8 19968862 downstream gene variant G/A snv 0.61 5
rs2331841 1.000 0.080 18 60161404 upstream gene variant G/A snv 0.43 5
rs2844479 0.925 0.200 6 31605179 intergenic variant A/C snv 0.34 5
rs4355801 0.882 0.120 8 118911634 regulatory region variant A/G;T snv 5
rs713586 0.925 0.160 2 24935139 intergenic variant T/C snv 0.58 5
rs10189761 0.882 0.120 2 646364 intergenic variant T/A snv 0.82 4
rs11152213 1.000 0.080 18 60185715 intergenic variant A/C;T snv 4
rs12463617 1.000 0.080 2 629244 regulatory region variant A/C;T snv 4
rs12955983 1.000 0.080 18 60205756 intergenic variant A/G snv 0.20 4
rs12969709 1.000 0.080 18 60192330 upstream gene variant C/A snv 0.21 4
rs13188458 0.882 0.160 5 8127718 intergenic variant T/G snv 0.22 4
rs17700144 1.000 0.080 18 60144750 intron variant G/A snv 0.14 4
rs17700633 0.882 0.120 18 60262199 intergenic variant G/A snv 0.28 4
rs2207139 1.000 0.080 6 50877777 intergenic variant A/G snv 0.16 4
rs545854 0.882 0.160 8 10002570 intron variant G/C snv 0.85 4
rs663129 0.882 0.160 18 60171168 intergenic variant G/A snv 0.24 4
rs9300039 0.851 0.160 11 41893816 intergenic variant C/A snv 9.8E-02 4
rs939583 1.000 0.080 2 622531 intergenic variant C/T snv 0.85 4