Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs10499194 0.752 0.400 6 137681500 intron variant C/T snv 0.24 10
rs2327832 0.790 0.320 6 137651931 intergenic variant A/G snv 0.16 10
rs2431697 0.776 0.240 5 160452971 intron variant T/C snv 0.44 10
rs2844511 0.807 0.200 6 31422007 intron variant A/G;T snv 10
rs3024505 0.790 0.320 1 206766559 upstream gene variant G/A snv 0.11 10
rs3130544 0.807 0.360 6 31090563 intergenic variant C/A snv 7.4E-02 10
rs11594656 0.776 0.240 10 6080046 intergenic variant T/A snv 0.18 9
rs1980422 0.776 0.320 2 203745673 intergenic variant C/A;T snv 9
rs2857595 0.827 0.320 6 31600692 intergenic variant G/A snv 0.27 9
rs9271366 0.807 0.240 6 32619077 intergenic variant G/A snv 0.86 9
rs2856718 0.790 0.360 6 32702478 downstream gene variant C/T snv 0.34 8
rs41295061 0.790 0.360 10 6072697 upstream gene variant C/A snv 6.1E-02 8
rs4324798 0.790 0.240 6 28808340 intergenic variant G/A snv 7.2E-02 8
rs4917014 0.807 0.360 7 50266267 upstream gene variant T/G snv 0.26 8
rs103294 0.827 0.200 19 54293995 downstream gene variant T/C snv 0.82 7
rs231726 0.790 0.200 2 203876143 downstream gene variant C/T snv 0.36 7
rs2647012 0.790 0.320 6 32696681 intergenic variant T/C snv 0.64 7
rs11117431 0.807 0.160 16 85981710 intron variant A/G snv 0.18 6
rs11117433 0.827 0.160 16 85985910 upstream gene variant G/A;C;T snv 6
rs1794282 0.807 0.320 6 32698749 intergenic variant C/T snv 6.4E-02 6
rs2254546 0.807 0.400 8 11486171 upstream gene variant A/G snv 0.83 6
rs3094054 0.807 0.280 6 30365728 upstream gene variant G/A;T snv 6
rs729302 0.827 0.160 7 128928906 intergenic variant A/C snv 0.28 6
rs7762279 0.807 0.360 6 32787513 intergenic variant T/C snv 8.4E-02 6
rs7812879 0.807 0.320 8 11482672 upstream gene variant T/A;C snv 6