Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs6822844 0.689 0.520 4 122588266 regulatory region variant G/T snv 0.10 20
rs2542151 0.763 0.480 18 12779948 upstream gene variant G/T snv 0.83 11
rs10499194 0.752 0.400 6 137681500 intron variant C/T snv 0.24 10
rs11209032 0.752 0.400 1 67274409 upstream gene variant G/A snv 0.30 10
rs1342326 0.790 0.360 9 6190076 intergenic variant A/C snv 0.21 9
rs1495965 0.790 0.280 1 67287825 intergenic variant C/T snv 0.55 8
rs6937506 0.807 0.280 6 132578260 intergenic variant G/A snv 0.25 7
rs10094579 0.807 0.280 8 89837077 downstream gene variant C/A snv 0.18 6
rs7775759 0.925 0.200 6 31384669 upstream gene variant G/A snv 0.36 6
rs913678 0.882 0.240 20 50338887 regulatory region variant T/C snv 0.51 6
rs17445836 0.851 0.320 16 85984057 intron variant G/A snv 0.15 5
rs4947296 0.851 0.440 6 31090401 intergenic variant T/A;C snv 5
rs6933050 0.925 0.200 6 31375855 non coding transcript exon variant T/C snv 0.22 5
rs9266409 0.925 0.200 6 31368791 intron variant T/C snv 0.22 5
rs11642873 0.851 0.280 16 85958099 intergenic variant A/C snv 0.15 4
rs2253907 0.882 0.360 6 31369093 intron variant C/T snv 0.43 3
rs924080 0.882 0.240 1 67294457 intergenic variant T/C snv 0.45 3
rs12119179 0.925 0.200 1 67281732 downstream gene variant A/C snv 0.30 2
rs76546355 0.925 0.200 6 31381371 downstream gene variant G/A snv 4.8E-02 2
rs10236188 1.000 0.200 7 150548168 intergenic variant T/C snv 0.49 1
rs10256482 1.000 0.200 7 150653887 intergenic variant T/C snv 0.47 1
rs10277380 1.000 0.200 7 150533604 intergenic variant T/A;C snv 1
rs10454134 1.000 0.200 2 48420887 TF binding site variant G/A snv 0.14 1
rs116799036 1.000 0.200 6 31381371 downstream gene variant G/A snv 1
rs11769828 1.000 0.200 7 150534221 intergenic variant C/T snv 0.19 1