Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs146052672 0.851 0.160 6 34242693 intron variant -/C delins 5
rs201739205 0.851 0.200 17 42552898 5 prime UTR variant A/C snv 7.8E-03 8.2E-03 5
rs35036378 0.851 0.200 14 64294403 5 prime UTR variant A/C snv 7.0E-03 5
rs1043307 0.776 0.360 12 121915890 missense variant A/C;G snv 14
rs35767 0.763 0.360 12 102481791 upstream gene variant A/C;G;T snv 13
rs7041
GC
0.576 0.800 4 71752617 missense variant A/C;T snv 0.52; 4.0E-06 64
rs10938397 0.851 0.200 4 45180510 intergenic variant A/G snv 0.37 19
rs1137100 0.627 0.640 1 65570758 missense variant A/G snv 0.30 0.25 39
rs1137101 0.554 0.760 1 65592830 missense variant A/G snv 0.51 0.50 77
rs1217691063 0.330 0.920 1 11796309 missense variant A/G snv 4.0E-06 7.0E-06 614
rs1269801977 0.925 0.120 2 169604087 missense variant A/G snv 4.0E-06 7.0E-06 4
rs1801252 0.724 0.320 10 114044277 missense variant A/G snv 0.15 0.17 17
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
rs2605100 1.000 0.080 1 219470882 intergenic variant A/G snv 0.77 3
rs268
LPL
0.637 0.480 8 19956018 missense variant A/G snv 1.3E-02 1.3E-02 41
rs3782889 0.851 0.160 12 110912851 intron variant A/G snv 7.1E-02 5
rs4757268 0.827 0.120 11 14789216 synonymous variant A/G snv 0.63 0.64 6
rs4994 0.578 0.640 8 37966280 missense variant A/G snv 0.11 9.2E-02 65
rs5498 0.531 0.760 19 10285007 missense variant A/G snv 0.44 0.37 99
rs699
AGT
0.501 0.800 1 230710048 missense variant A/G snv 0.55 0.58 134
rs16998073 0.925 0.120 4 80263187 upstream gene variant A/G;T snv 10
rs5068 0.776 0.160 1 11845917 3 prime UTR variant A/G;T snv 13
rs34104384
LEP
0.851 0.200 7 128241254 upstream gene variant A/T snv 8.2E-03 5
rs3764261 0.732 0.280 16 56959412 upstream gene variant C/A snv 0.31 26