Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs2526378 0.925 0.120 17 58326988 intron variant A/G snv 0.51 2
rs2965169 0.925 0.120 19 44747899 non coding transcript exon variant A/C snv 0.50 2
rs7396366 0.925 0.120 11 986185 intron variant C/A snv 0.58 2
rs8003602 0.925 0.120 14 99682624 upstream gene variant T/C snv 0.67 2
rs747760223 0.882 0.120 3 39412034 missense variant T/C snv 4.0E-06 7.0E-06 3
rs908832 0.851 0.120 9 137018032 missense variant A/C;G snv 0.97 0.96 4
rs2234246 0.827 0.240 6 41276002 3 prime UTR variant C/T snv 0.44 5
rs4769874 0.827 0.240 13 30752304 intron variant G/A snv 5.8E-02 5
rs8100239 0.882 0.200 19 44749847 intron variant T/A snv 0.38 5
rs1051338 0.807 0.120 10 89247603 missense variant T/G snv 0.32 0.26 7
rs2066715 0.807 0.160 9 104825752 missense variant C/T snv 8.2E-02 5.5E-02 7
rs1035071612 0.763 0.240 19 11113361 missense variant C/A;T snv 4.0E-06 9
rs146292819 0.790 0.240 9 104794495 missense variant T/G snv 2.9E-04 3.8E-04 9
rs4149313 0.763 0.240 9 104824472 missense variant T/C snv 9
rs4717806 0.776 0.200 7 73702147 intron variant T/A;C snv 9
rs5174 0.776 0.240 1 53247055 missense variant C/T snv 0.29 0.28 10
rs6859 0.827 0.120 19 44878777 3 prime UTR variant A/G snv 0.58 10
rs1803274 0.763 0.360 3 165773492 missense variant C/T snv 0.18 0.18 13
rs2066714 0.742 0.240 9 104824472 missense variant T/C snv 0.21 0.25 13
rs2227631 0.742 0.200 7 101126257 upstream gene variant A/G snv 0.54 13
rs7044343 0.752 0.520 9 6254208 intron variant C/T snv 0.51 13
rs2227564 0.763 0.320 10 73913343 missense variant T/C snv 0.75 0.81 15
rs2016520 0.752 0.320 6 35411001 5 prime UTR variant C/T snv 0.78 16
rs4646 0.716 0.360 15 51210647 3 prime UTR variant A/C snv 0.67 0.70 16
rs688 0.742 0.400 19 11116926 synonymous variant C/T snv 0.39 0.34 16