Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs10129035 12 83706429 intergenic variant T/A;C snv 1
rs10158210 1 158342195 intergenic variant A/G;T snv 1
rs1016680 17 37514283 downstream gene variant A/C snv 0.74 1
rs1023667 5 158541893 intron variant G/A;C snv 1
rs10252662 7 44771624 downstream gene variant C/T snv 0.37 1
rs1037117 15 101528455 upstream gene variant G/A snv 0.28 1
rs10494322 1 159367158 intron variant T/C snv 0.15 1
rs10752632 1 159905665 downstream gene variant G/A snv 0.54 1
rs10772108 12 9746454 intergenic variant C/G;T snv 1
rs10797857 1 183175588 intergenic variant C/A;G snv 1
rs10808536 8 86156820 upstream gene variant G/A snv 0.26 1
rs1082428 6 137886592 downstream gene variant C/G;T snv 1
rs10858963 12 90152611 intergenic variant T/A;C snv 1
rs10883756 10 102640355 upstream gene variant T/A;C snv 1
rs10889574 1 65683658 intergenic variant G/A snv 0.34 1
rs10908581 1 157668485 intergenic variant A/G;T snv 1
rs10908584 1 157671968 downstream gene variant T/A;G snv 1
rs10908702 1 159258588 intergenic variant C/T snv 0.46 1
rs10908709 1 159350390 intron variant C/A snv 0.34 1
rs10908714 1 159370563 intron variant T/A snv 0.38 1
rs10918341 1 161980609 downstream gene variant A/G snv 0.51 1
rs10918342 1 161980661 downstream gene variant G/A snv 0.51 1
rs10935478 3 98709311 non coding transcript exon variant C/T snv 0.37 1
rs10961195 9 13676534 intron variant T/C snv 0.50 1
rs10973700 9 38196120 regulatory region variant G/C snv 0.49 1