Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs2736340 0.683 0.480 8 11486464 upstream gene variant C/T snv 0.25 22
rs6822844 0.689 0.520 4 122588266 regulatory region variant G/T snv 0.10 20
rs4728142 0.732 0.320 7 128933913 upstream gene variant G/A snv 0.38 18
rs35705950 0.763 0.240 11 1219991 splice region variant G/A;T snv 14
rs6920220 0.742 0.440 6 137685367 intron variant G/A snv 0.16 14
rs204999 0.763 0.480 6 32142202 intergenic variant A/G snv 0.28 13
rs6457617 0.763 0.480 6 32696074 intergenic variant C/A;T snv 11
rs10499194 0.752 0.400 6 137681500 intron variant C/T snv 0.24 10
rs2248462 0.807 0.240 6 31479019 downstream gene variant G/A snv 0.19 10
rs11594656 0.776 0.240 10 6080046 intergenic variant T/A snv 0.18 9
rs3129763 0.827 0.280 6 32623148 TF binding site variant G/A snv 0.23 6
rs9275312 0.807 0.280 6 32697951 intergenic variant A/G snv 0.16 6
rs2431098 0.827 0.240 5 160460329 intron variant A/G;T snv 5
rs2736337 0.827 0.240 8 11484371 upstream gene variant T/C snv 0.26 5
rs35929052 0.827 0.160 16 85960878 downstream gene variant C/G;T snv 5
rs8182352 0.827 0.160 17 5651667 intergenic variant T/C snv 0.44 5
rs9275224 0.851 0.200 6 32692101 TF binding site variant A/G snv 0.53 5
rs11117432 0.851 0.200 16 85985665 upstream gene variant G/A snv 0.15 4
rs112846137 0.851 0.160 3 160595133 intergenic variant G/T snv 5.3E-02 4
rs11642873 0.851 0.280 16 85958099 intergenic variant A/C snv 0.15 4
rs12711490 0.925 0.080 16 85939422 intron variant T/C snv 0.18 4
rs193107685 0.851 0.160 7 74123572 downstream gene variant T/C snv 1.0E-02 4
rs5000634 0.851 0.200 6 32695787 intergenic variant A/G snv 0.39 4
rs58721818 0.851 0.160 6 137922602 regulatory region variant C/G;T snv 4
rs744600 0.851 0.160 2 190700031 intron variant G/T snv 0.60 4