Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs13101828 0.851 0.160 4 971932 intron variant A/G snv 0.43 6
rs148704956 0.716 0.360 6 52187772 missense variant A/G snv 8.0E-06 7.0E-06 19
rs1800625 0.641 0.680 6 32184665 upstream gene variant A/G snv 0.15 39
rs1800682 0.637 0.440 10 88990206 non coding transcript exon variant A/G snv 0.54 32
rs1800871 0.508 0.800 1 206773289 5 prime UTR variant A/G snv 0.69 108
rs1801394 0.531 0.840 5 7870860 missense variant A/G snv 0.47 0.45 101
rs1805087
MTR
0.496 0.800 1 236885200 missense variant A/G snv 0.20 0.21 135
rs187084 0.641 0.480 3 52227015 intron variant A/G snv 0.38 36
rs1913517 0.925 0.120 10 48911009 intron variant A/G snv 0.54 2
rs2248932
BLK
0.882 0.160 8 11534141 intron variant A/G snv 0.60 3
rs2277798 0.925 0.120 21 42403997 missense variant A/G snv 0.55 0.60 3
rs2283790 0.882 0.120 22 21602364 intron variant A/G snv 0.21 3
rs2327832 0.790 0.320 6 137651931 intergenic variant A/G snv 0.16 10
rs2476601 0.498 0.800 1 113834946 missense variant A/G snv 0.93 0.93 121
rs2844635 0.882 0.200 6 31107704 downstream gene variant A/G snv 0.37 3
rs2858331 0.827 0.240 6 32713500 upstream gene variant A/G snv 0.42 5
rs3077 0.701 0.440 6 33065245 3 prime UTR variant A/G snv 0.29 16
rs3129939 0.827 0.360 6 32368989 intron variant A/G snv 0.14 5
rs3129943 0.851 0.240 6 32370918 intron variant A/G snv 0.26 4
rs3129963 0.851 0.280 6 32412431 downstream gene variant A/G snv 0.17 4
rs3130299 0.851 0.240 6 32235760 regulatory region variant A/G snv 0.24 4
rs3135394 0.851 0.240 6 32440720 intron variant A/G snv 6.3E-02 4
rs3746444 0.514 0.760 20 34990448 mature miRNA variant A/G snv 0.20 0.19 105
rs3819024 0.701 0.560 6 52185988 upstream gene variant A/G snv 0.34 17
rs389884 0.776 0.440 6 31973120 non coding transcript exon variant A/G snv 7.1E-02 10