Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1569723 0.851 0.280 20 46113425 upstream gene variant C/A snv 0.80 6
rs2515919 1.000 6 31596390 upstream gene variant A/G snv 0.31 5
rs13212562 0.925 0.120 6 27332531 intergenic variant A/G snv 0.13 4
rs10129426 14 103552118 upstream gene variant G/A snv 0.54 2
rs10192369 2 160524377 intergenic variant G/A snv 0.45 2
rs10789285 1.000 0.040 1 69322799 intergenic variant T/G snv 0.33 2
rs10922907 1 90727492 downstream gene variant A/G;T snv 2
rs10937921 1.000 0.120 4 3274764 downstream gene variant C/T snv 0.40 2
rs1107960 14 54917622 intergenic variant T/A snv 0.42 2
rs11793831 9 23362313 intron variant G/A;T snv 2
rs12028010 1 41298799 intron variant T/C snv 0.19 2
rs12069733 1.000 0.040 1 43475837 TF binding site variant G/A snv 0.37 2
rs13259607 8 70439812 intergenic variant C/T snv 0.15 2
rs1343775 1 41292321 intron variant A/G snv 0.17 2
rs142601917 12 120914271 upstream gene variant C/A;G;T snv 2
rs1430055 2 16499521 intergenic variant G/A snv 0.61 2
rs1473634 8 21057805 intron variant A/G snv 0.22 2
rs1492014 3 94352637 intergenic variant T/C;G snv 2
rs17245822 13 72557556 intergenic variant A/C snv 0.34 2
rs2523587 1.000 0.040 6 31359623 upstream gene variant T/C snv 0.71 2
rs258951 5 92718160 intergenic variant T/A snv 0.55 2
rs4484297 4 16330759 downstream gene variant G/C snv 0.31 2
rs5757673 22 39441915 downstream gene variant T/C snv 0.79 2
rs6492538 13 91341492 intergenic variant A/C snv 0.83 2
rs6518724 22 31008409 intergenic variant C/G;T snv 2