Source: GWASCAT

Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs7679673 0.677 0.440 4 105140377 intron variant C/A snv 0.50 23
rs115707823 0.701 0.320 6 30374976 intergenic variant G/A snv 19
rs247617 0.827 0.160 16 56956804 regulatory region variant C/A snv 0.29 18
rs1728918 0.827 0.160 2 27412596 upstream gene variant A/G;T snv 18
rs765547 0.827 0.160 8 20008763 intergenic variant G/A;C;T snv 17
rs562338 0.807 0.160 2 21065449 intergenic variant A/G snv 0.69 17
rs7703051 0.851 0.120 5 75329662 intron variant C/A snv 0.38 17
rs635634 0.882 0.160 9 133279427 upstream gene variant T/A;C snv 17
rs141752671 0.708 0.280 11 103745837 intron variant A/G snv 5.4E-03 17
rs11907546 0.708 0.280 20 34131991 upstream gene variant C/A;T snv 17
rs7931342 0.689 0.360 11 69227030 intergenic variant T/G snv 0.58 17
rs147527678 0.708 0.280 6 32699696 intergenic variant G/A;C snv 17
rs148883465 0.708 0.280 11 103813371 intron variant A/G snv 7.2E-03 17
rs147680653 0.708 0.280 6 29785031 intergenic variant A/G snv 17
rs1862626 0.708 0.280 5 56737113 regulatory region variant G/T snv 0.68 17
rs186507655 0.708 0.280 1 1351675 upstream gene variant G/A snv 6.8E-03 17
rs12420422 0.851 0.120 11 123009573 intergenic variant G/A snv 3.4E-02 16
rs6533530 0.851 0.120 4 110810780 intergenic variant T/C snv 0.47 16
rs799165 0.851 0.120 7 73637727 intergenic variant T/A snv 0.13 16
rs222826 0.851 0.120 2 146120964 regulatory region variant T/C snv 0.94 16
rs478442 0.851 0.120 2 21176344 intergenic variant G/C;T snv 16
rs2866611 0.851 0.120 20 41322165 upstream gene variant A/T snv 0.58 16
rs12310617 0.851 0.120 12 3060327 intergenic variant C/T snv 0.11 16
rs17140821 0.851 0.120 7 19177581 regulatory region variant G/A snv 7.9E-02 16
rs8082812 0.851 0.120 18 8522684 intergenic variant C/A snv 4.6E-02 16