Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs562338 0.807 0.160 2 21065449 intergenic variant A/G snv 0.69 21
rs247617 0.827 0.160 16 56956804 regulatory region variant C/A snv 0.29 20
rs1728918 0.827 0.160 2 27412596 upstream gene variant A/G;T snv 19
rs478442 0.851 0.120 2 21176344 intergenic variant G/C;T snv 18
rs765547 0.827 0.160 8 20008763 intergenic variant G/A;C;T snv 18
rs7703051 0.851 0.120 5 75329662 intron variant C/A snv 0.38 18
rs799165 0.851 0.120 7 73637727 intergenic variant T/A snv 0.13 17
rs12310617 0.851 0.120 12 3060327 intergenic variant C/T snv 0.11 16
rs12420422 0.851 0.120 11 123009573 intergenic variant G/A snv 3.4E-02 16
rs17140821 0.851 0.120 7 19177581 regulatory region variant G/A snv 7.9E-02 16
rs222826 0.851 0.120 2 146120964 regulatory region variant T/C snv 0.94 16
rs2866611 0.851 0.120 20 41322165 upstream gene variant A/T snv 0.58 16
rs2980853 0.851 0.120 8 125466108 upstream gene variant A/C snv 0.43 16
rs6533530 0.851 0.120 4 110810780 intergenic variant T/C snv 0.47 16
rs8082812 0.851 0.120 18 8522684 intergenic variant C/A snv 4.6E-02 16
rs2794520 0.807 0.240 1 159709026 upstream gene variant C/A;T snv 9
rs9942416 5 75741470 intergenic variant C/G snv 0.53 9
rs10096633 1.000 0.040 8 19973410 regulatory region variant C/T snv 0.22 8
rs1495743 8 18415790 intergenic variant G/A;C snv 6
rs10244051 1.000 0.080 7 15024208 intergenic variant T/A;G snv 3
rs12753193 1 65703996 non coding transcript exon variant G/A snv 0.58 3
rs1558318 1.000 0.080 7 15025987 intergenic variant A/T snv 0.55 3
rs10799701 1 21494497 intergenic variant A/G snv 0.47 2
rs10965246 9 22132699 downstream gene variant T/C snv 0.15 2
rs1203936 20 22611792 upstream gene variant G/C;T snv 2