Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs12144049 1.000 0.120 1 152468434 intergenic variant C/G;T snv 1
rs12153855 0.776 0.320 6 32107027 intron variant T/C snv 0.11 11
rs1217691063 0.330 0.920 1 11796309 missense variant A/G snv 4.0E-06 7.0E-06 614
rs12188917 1.000 0.120 5 132655393 intron variant T/C;G snv 1
rs121909626 0.882 0.120 1 152307225 stop gained G/C;T snv 2.0E-05 4
rs12198173 0.827 0.240 6 32059031 intron variant G/A snv 0.10 9
rs12211410 0.925 0.120 6 32081646 missense variant C/G;T snv 5.6E-05; 7.7E-02; 3.7E-05 5
rs1221479287 0.925 0.120 19 54783499 missense variant G/A snv 7.0E-06 2
rs1239828657 0.925 0.120 9 6256028 missense variant T/G snv 4.0E-06 2
rs12568784 0.925 0.120 1 152350656 stop gained G/A;T snv 0.24 0.21 2
rs12634229 0.882 0.120 3 112657461 intergenic variant T/C snv 0.15 3
rs1295685 0.790 0.160 5 132660753 3 prime UTR variant A/G snv 0.81 7
rs1295686 0.882 0.160 5 132660151 intron variant T/A;C snv 0.68 7
rs13015714 0.882 0.200 2 102355405 intron variant G/T snv 0.77 3
rs13132933 0.925 0.200 4 122089432 upstream gene variant T/C snv 0.22 2
rs13139310 0.925 0.120 4 184435757 intron variant G/A;C snv 3
rs13199524 0.807 0.240 6 32098988 intron variant C/T snv 8.4E-02 9
rs1335908042 0.925 0.120 2 112918756 missense variant T/G snv 4.0E-06 2
rs13360927 0.882 0.160 5 110700055 intron variant A/G snv 9.3E-02 3
rs13361382 0.882 0.160 5 110713253 intron variant G/A snv 9.3E-02 3
rs1343795 0.882 0.120 17 49334880 intron variant C/A snv 0.78 5
rs1384974 0.925 0.120 3 177009491 downstream gene variant T/C snv 9.6E-02 2
rs138726443 0.790 0.200 1 152307547 stop gained G/A;C;T snv 2.8E-03; 4.0E-06; 1.6E-05 7
rs1422985 0.925 0.120 5 148114596 intron variant A/C snv 3.2E-02 2
rs1443712053 0.925 0.120 1 152310672 stop gained G/C snv 4.0E-06 2