Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs579459 0.752 0.320 9 133278724 upstream gene variant C/T snv 0.81 28
rs7679673 0.677 0.440 4 105140377 intron variant C/A snv 0.50 28
rs495828 0.827 0.200 9 133279294 upstream gene variant T/G snv 0.81 24
rs2853961 6 31264212 downstream gene variant G/A snv 0.38 13
rs28601761 1.000 0.040 8 125487789 intron variant C/G snv 0.37 13
rs10821907 0.776 0.080 10 50888694 upstream gene variant C/T snv 0.20 12
rs9494145 0.925 0.080 6 135111414 intergenic variant T/A;C snv 11
rs12509595 1.000 0.080 4 80261400 intergenic variant T/C snv 0.23 10
rs218265 4 54542832 intergenic variant T/C snv 0.21 10
rs10857147 1.000 0.040 4 80259918 intergenic variant A/T snv 0.25 9
rs62435145 1.000 0.040 7 1246931 regulatory region variant G/T snv 0.51 8
rs17534202 1.000 0.120 1 203312047 downstream gene variant G/C snv 0.40 7
rs737092 20 57415349 regulatory region variant T/C snv 0.58 7
rs12216125 0.925 0.120 6 25997230 intron variant C/T snv 0.26 6
rs130624 22 37042611 regulatory region variant G/T snv 0.47 6
rs13125101 4 80253438 TF binding site variant G/A snv 0.24 6
rs1533988 7 1253374 intergenic variant A/T snv 0.59 6
rs218237 4 54528005 intergenic variant C/T snv 0.18 6
rs592423 6 139519556 intron variant A/C snv 0.50 6
rs605066 6 139508529 intron variant C/T snv 0.53 6
rs7753826 0.925 0.120 6 26042011 upstream gene variant T/A;C snv 6
rs1150660 0.925 0.120 6 26101212 upstream gene variant A/C snv 0.73 5
rs13194491 1.000 0.040 6 27069301 intergenic variant C/T snv 4.8E-02 5
rs1320963 6 135122074 intergenic variant A/G snv 0.35 5
rs198833 6 26114280 downstream gene variant G/A snv 0.87 5