Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1024611 0.568 0.800 17 34252769 upstream gene variant A/G snv 0.28 63
rs7679673 0.677 0.440 4 105140377 intron variant C/A snv 0.50 28
rs7931342 0.689 0.360 11 69227030 intergenic variant T/G snv 0.58 20
rs115707823 0.701 0.320 6 30374976 intergenic variant G/A snv 19
rs11907546 0.708 0.280 20 34131991 upstream gene variant C/A;T snv 17
rs141752671 0.708 0.280 11 103745837 intron variant A/G snv 5.4E-03 17
rs147527678 0.708 0.280 6 32699696 intergenic variant G/A;C snv 17
rs147680653 0.708 0.280 6 29785031 intergenic variant A/G snv 17
rs148883465 0.708 0.280 11 103813371 intron variant A/G snv 7.2E-03 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
rs874945 0.732 0.240 12 53961667 upstream gene variant C/T snv 0.38 14
rs2660753 0.790 0.240 3 87061524 intergenic variant T/C snv 0.76 9
rs3814113 0.827 0.200 9 16915023 upstream gene variant T/C snv 0.41 5
rs67397200 0.827 0.160 19 17290595 upstream gene variant C/G snv 0.27 5
rs6785617 0.882 0.120 3 172501054 downstream gene variant A/T snv 3.7E-02 4
rs7313833 0.851 0.120 12 27930263 intergenic variant G/A snv 0.37 4
rs10962692 0.925 0.120 9 16915876 upstream gene variant G/A;C snv 3
rs4954956 0.882 0.120 2 138787007 regulatory region variant C/T snv 0.25 3
rs62274041 0.925 0.120 3 156717851 upstream gene variant G/A;T snv 3
rs7365052 0.882 0.120 1 236786561 intergenic variant T/C snv 3
rs7748275 0.882 0.120 6 3580855 downstream gene variant T/A snv 8.2E-02 3
rs4691139 1.000 0.120 4 164987569 non coding transcript exon variant A/G;T snv 2
rs10674174 1.000 0.120 13 61317942 intergenic variant -/G ins 1
rs10899426 1.000 0.120 11 78008566 intergenic variant T/C snv 3.3E-02 1