Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs10006237 4 136606920 intergenic variant C/T snv 0.50 1
rs10009397 4 28695228 intergenic variant A/T snv 0.89 1
rs10026457 4 58384912 intergenic variant T/G snv 0.71 1
rs10061387 5 124524355 intron variant A/G snv 0.47 1
rs10109012 8 15387338 intergenic variant C/T snv 0.52 1
rs10114066 9 73908824 intergenic variant T/A snv 0.76 1
rs1016162 3 102299 regulatory region variant C/T snv 0.36 1
rs10164820 2 100433891 intergenic variant G/C snv 0.20 1
rs1016678 17 37514090 downstream gene variant A/G snv 0.72 1
rs10177638 2 62659875 intron variant C/T snv 0.69 1
rs10196515 2 153383795 intergenic variant C/A snv 0.82 1
rs10197780 2 62646060 intron variant T/C snv 0.78 1
rs10223255 5 92705821 intergenic variant A/C;G snv 1
rs10267100 7 115386686 intergenic variant T/G snv 0.67 1
rs10275833 7 1761060 regulatory region variant T/C snv 0.31 1
rs1028772 13 55028648 intergenic variant A/G snv 0.50 1
rs1037144 1 159598058 upstream gene variant G/A snv 0.51 1
rs10450860 13 83985362 intergenic variant G/A snv 0.25 1
rs10472030 5 58015731 intergenic variant C/T snv 0.23 1
rs10473629 5 23217458 intergenic variant G/A snv 0.42 1
rs10497215 2 160714470 intergenic variant T/C snv 0.46 1
rs1073090 1 96023656 downstream gene variant G/A snv 0.17 1
rs10740140 10 63759994 intron variant A/C;G;T snv 1
rs1074462 5 109607295 intergenic variant A/T snv 0.52 1
rs10750539 11 133678978 intergenic variant G/A snv 0.30 1