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
rs11206510 0.763 0.240 1 55030366 intergenic variant T/A;C;G snv 16
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
rs2200733 0.752 0.240 4 110789013 intergenic variant C/T snv 0.18 12
rs1458038 0.925 0.120 4 80243569 intergenic variant C/T snv 0.23 10
rs2431697 0.776 0.240 5 160452971 intron variant T/C snv 0.44 10
rs10033464 0.807 0.200 4 110799605 downstream gene variant T/G snv 0.86 8
rs460976 0.851 0.120 21 41463567 downstream gene variant A/G;T snv 7
rs1906591 0.851 0.200 4 110787733 intergenic variant G/A snv 0.15 5
rs13143308 0.882 0.120 4 110793263 upstream gene variant T/C;G snv 4
rs499818 0.851 0.080 6 13332235 upstream gene variant G/A snv 0.21 4
rs6817105 0.882 0.080 4 110784612 intergenic variant T/C snv 0.19 3