Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1131691014 0.439 0.800 17 7676154 frameshift variant -/C ins 213
rs3783553 0.667 0.480 2 112774138 3 prime UTR variant -/TGAA delins 26
rs1990172 0.827 0.120 7 20164512 intron variant A/C snv 0.27 6
rs712 0.677 0.360 12 25209618 3 prime UTR variant A/C snv 0.46 24
rs7763881 0.776 0.160 6 8653014 non coding transcript exon variant A/C snv 0.44 11
rs17879961 0.597 0.480 22 28725099 missense variant A/C;G snv 4.1E-03 45
rs2273535 0.645 0.360 20 56386485 missense variant A/C;T snv 0.28 37
rs7041
GC
0.576 0.800 4 71752617 missense variant A/C;T snv 0.52; 4.0E-06 61
rs1128503 0.564 0.760 7 87550285 synonymous variant A/G snv 0.54 0.63 64
rs11615 0.572 0.640 19 45420395 synonymous variant A/G snv 0.50 0.55 62
rs1217691063 0.330 0.920 1 11796309 missense variant A/G snv 4.0E-06 7.0E-06 614
rs1695 0.457 0.880 11 67585218 missense variant A/G snv 0.34 0.36 187
rs1800682 0.637 0.440 10 88990206 non coding transcript exon variant A/G snv 0.54 25
rs1801394 0.531 0.840 5 7870860 missense variant A/G snv 0.47 0.45 101
rs2241880 0.627 0.600 2 233274722 missense variant A/G snv 0.45 0.44 36
rs2274223 0.620 0.400 10 94306584 missense variant A/G snv 0.28 0.31 39
rs2853669 0.649 0.320 5 1295234 upstream gene variant A/G snv 0.25 35
rs3742330 0.662 0.640 14 95087025 3 prime UTR variant A/G snv 8.7E-02 24
rs3746444 0.514 0.760 20 34990448 mature miRNA variant A/G snv 0.20 0.19 105
rs4135385 0.742 0.320 3 41237949 non coding transcript exon variant A/G snv 0.19 14
rs4444903
EGF
0.630 0.360 4 109912954 5 prime UTR variant A/G snv 0.51 35
rs5498 0.531 0.760 19 10285007 missense variant A/G snv 0.44 0.37 97
rs750521832 0.732 0.200 11 102718452 missense variant A/G snv 4.0E-06 14
rs1045642 0.456 0.840 7 87509329 synonymous variant A/G;T snv 0.50 214
rs121913279 0.526 0.560 3 179234297 missense variant A/G;T snv 4.0E-06; 4.0E-06 62