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
rs17782313 0.683 0.480 18 60183864 intergenic variant T/C snv 0.24 34
rs7679673 0.677 0.440 4 105140377 intron variant C/A snv 0.50 28
rs12826786 0.683 0.480 12 53961717 upstream gene variant C/T snv 0.38 26
rs10811661 0.724 0.400 9 22134095 intergenic variant T/C snv 0.14 22
rs2046210 0.708 0.280 6 151627231 intergenic variant G/A snv 0.41 21
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
rs642961 0.732 0.440 1 209815925 intergenic variant A/G snv 0.84 14
rs874945 0.732 0.240 12 53961667 upstream gene variant C/T snv 0.38 14
rs889312 0.732 0.360 5 56736057 regulatory region variant C/A snv 0.69 14
rs10811474 0.742 0.240 9 21114238 intergenic variant A/G snv 0.44 11
rs10941679 0.763 0.120 5 44706396 intergenic variant A/G snv 0.25 11
rs13293512 0.763 0.360 9 94167461 intron variant T/C snv 0.24 11
rs1111875 0.776 0.360 10 92703125 intergenic variant C/T snv 0.36 10
rs7794030 0.776 0.120 7 38712494 intergenic variant A/G snv 0.23 10
rs9834244 0.776 0.120 3 151704793 intergenic variant G/A snv 6.1E-02 10
rs2069514 0.807 0.160 15 74745879 upstream gene variant G/A snv 0.13 9