Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs653178 0.672 0.600 12 111569952 intron variant C/T snv 0.67 17
rs2476601 0.498 0.800 1 113834946 missense variant A/G snv 0.93 0.93 13
rs8321 0.742 0.320 6 30064745 3 prime UTR variant A/C snv 5.4E-02 5.9E-02 11
rs3130380 0.807 0.280 6 30311353 intron variant G/A snv 6.6E-02 10
rs2187668 0.701 0.480 6 32638107 intron variant C/T snv 3.3E-03 10
rs9261290 0.807 0.280 6 30070870 3 prime UTR variant T/C;G snv 5.2E-02; 7.2E-06 10
rs9275572 0.724 0.360 6 32711222 upstream gene variant A/G;T snv 9
rs3099844 0.732 0.400 6 31481199 non coding transcript exon variant C/A snv 0.11 9
rs9271366 0.807 0.240 6 32619077 intergenic variant G/A snv 0.86 8
rs7574865 0.574 0.720 2 191099907 intron variant T/G snv 0.79 8
rs185819 0.851 0.200 6 32082290 missense variant T/A;C;G snv 8.2E-06; 0.58; 4.1E-06 8
rs2269426 0.807 0.280 6 32108722 intron variant G/A snv 0.35 8
rs2736340 0.683 0.480 8 11486464 upstream gene variant C/T snv 0.25 7
rs2844511 0.807 0.200 6 31422007 intron variant A/G;T snv 7
rs6457374 0.851 0.200 6 31304484 intron variant C/T snv 0.81 7
rs886424 0.776 0.320 6 30814225 non coding transcript exon variant C/T snv 7.1E-02 8.7E-02 7
rs389884 0.776 0.440 6 31973120 non coding transcript exon variant A/G snv 7.1E-02 7
rs10488631 0.742 0.280 7 128954129 upstream gene variant T/C snv 9.0E-02 7
rs1794282 0.807 0.320 6 32698749 intergenic variant C/T snv 6.4E-02 6
rs2327832 0.790 0.320 6 137651931 intergenic variant A/G snv 0.16 6
rs2857595 0.827 0.320 6 31600692 intergenic variant G/A snv 0.27 6
rs3024505 0.790 0.320 1 206766559 upstream gene variant G/A snv 0.11 6
rs3130544 0.807 0.360 6 31090563 intergenic variant C/A snv 7.4E-02 6
rs6920220 0.742 0.440 6 137685367 intron variant G/A snv 0.16 6
rs7762279 0.807 0.360 6 32787513 intergenic variant T/C snv 8.4E-02 6