Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs10946398 0.827 0.160 6 20660803 intron variant A/C snv 0.40 7
rs1333048 0.683 0.320 9 22125348 intron variant A/C snv 0.44 24
rs854560 0.513 0.800 7 95316772 missense variant A/C;G;N;T snv 0.29 113
rs2032582 0.538 0.800 7 87531302 missense variant A/C;T snv 0.54; 3.8E-02 97
rs2228145 0.602 0.720 1 154454494 missense variant A/C;T snv 0.38; 1.2E-05 57
rs7041
GC
0.576 0.800 4 71752617 missense variant A/C;T snv 0.52; 4.0E-06 64
rs1217691063 0.330 0.920 1 11796309 missense variant A/G snv 4.0E-06 7.0E-06 614
rs1467568 0.776 0.320 10 67915401 intron variant A/G snv 0.46 8
rs1695 0.457 0.880 11 67585218 missense variant A/G snv 0.34 0.36 188
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
rs20455 0.763 0.160 6 39357302 missense variant A/G snv 0.41 0.49 12
rs2075650 0.662 0.360 19 44892362 intron variant A/G snv 0.13 0.13 45
rs268
LPL
0.637 0.480 8 19956018 missense variant A/G snv 1.3E-02 1.3E-02 41
rs372359132 0.827 0.160 5 7878203 missense variant A/G snv 4.0E-06 2.1E-05 5
rs3774261 0.776 0.320 3 186853770 splice region variant A/G snv 0.55 10
rs3782889 0.851 0.160 12 110912851 intron variant A/G snv 7.1E-02 5
rs4420638 0.708 0.520 19 44919689 downstream gene variant A/G snv 0.18 43
rs4880 0.500 0.840 6 159692840 missense variant A/G snv 0.48 0.47 131
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
rs9340799 0.583 0.680 6 151842246 intron variant A/G snv 0.32 62
rs16998073 0.925 0.120 4 80263187 upstream gene variant A/G;T snv 10
rs7649121 0.882 0.160 3 186850996 intron variant A/T snv 0.17 3