Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs104895271 0.851 0.240 12 6334161 missense variant A/C;G snv 1.6E-04; 4.8E-05 6
rs1678542 0.790 0.320 12 57574932 intron variant C/G snv 0.42 9
rs767455 0.742 0.400 12 6341779 synonymous variant T/C snv 0.37 0.40 13
rs10892279 1.000 0.120 11 118741072 intron variant G/A;T snv 0.25 3
rs11221332 0.763 0.280 11 128511079 intron variant C/A;T snv 13
rs150240657 0.925 0.120 11 47682026 missense variant G/A snv 8.7E-05 3.6E-04 3
rs4409785 0.752 0.240 11 95578258 intron variant T/C snv 0.13 12
rs2104286 0.662 0.440 10 6057082 intron variant T/C snv 0.18 25
rs4750316 0.882 0.160 10 6351298 non coding transcript exon variant C/G;T snv 5
rs706778 0.695 0.320 10 6056986 intron variant C/T snv 0.46 19
rs71508903 0.807 0.160 10 62020112 intron variant C/T snv 0.15 7
rs1953126 1.000 0.120 9 120878222 intron variant T/C snv 0.68 3
rs3761847 0.827 0.200 9 120927961 intron variant G/A snv 0.52 8
rs6478109 0.752 0.320 9 114806486 upstream gene variant A/G snv 0.74 12
rs951005 0.807 0.200 9 34743684 intron variant G/A snv 0.78 10
rs13277113
BLK
0.695 0.520 8 11491677 intron variant G/A snv 0.25 18
rs2736340 0.683 0.480 8 11486464 upstream gene variant C/T snv 0.25 22
rs10488631 0.742 0.280 7 128954129 upstream gene variant T/C snv 9.0E-02 13
rs10954213 0.752 0.200 7 128949373 3 prime UTR variant G/A snv 0.58 11
rs13447 0.882 0.200 7 75166663 non coding transcript exon variant T/A;C snv 1.9E-02 4
rs1800795 0.494 0.840 7 22727026 intron variant C/G snv 0.71 140
rs2004640 0.662 0.520 7 128938247 splice donor variant T/G snv 0.52 26
rs201802880 0.882 0.200 7 74779296 missense variant G/A snv 1.1E-03 4
rs1738074 0.790 0.320 6 159044945 5 prime UTR variant T/C snv 0.49 9
rs2070600 0.561 0.760 6 32183666 missense variant C/T snv 5.3E-02 3.6E-02 82