Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1333048 0.683 0.320 9 22125348 intron variant A/C snv 0.44 7
rs11216126 1.000 0.040 11 116746524 downstream gene variant A/C snv 0.11 3
rs12988520 1.000 0.040 2 233698748 intron variant A/C snv 0.51 2
rs1797912 1.000 0.040 3 12428740 intron variant A/C snv 0.33 2
rs295
LPL
1.000 0.040 8 19958727 intron variant A/C snv 0.28 1
rs8179252 0.882 0.120 2 27523965 downstream gene variant A/C snv 0.37 1
rs2943634 0.763 0.200 2 226203364 intergenic variant A/C;G snv 5
rs6589567 1.000 0.040 11 116799960 intergenic variant A/C;G;T snv 3
rs1441756 1.000 0.040 8 20010875 intergenic variant A/C;G;T snv 1
rs2228145 0.602 0.720 1 154454494 missense variant A/C;T snv 0.38; 1.2E-05 7
rs180349 0.925 0.200 11 116741111 intergenic variant A/C;T snv 3
rs7041
GC
0.576 0.800 4 71752617 missense variant A/C;T snv 0.52; 4.0E-06 3
rs8192284 0.724 0.720 1 154454494 missense variant A/C;T snv 3
rs13022873 0.882 0.120 2 27592643 intron variant A/C;T snv 2
rs2237895 0.790 0.240 11 2835964 intron variant A/C;T snv 1
rs486394 1.000 0.040 11 116655605 intron variant A/C;T snv 1
rs1535 0.752 0.240 11 61830500 intron variant A/G snv 0.31 18
rs10938397 0.851 0.200 4 45180510 intergenic variant A/G snv 0.37 8
rs9987289 1.000 0.040 8 9325848 non coding transcript exon variant A/G snv 0.87 8
rs929596 0.925 0.040 2 233765830 intron variant A/G snv 0.32 7
rs11708067 0.882 0.080 3 123346931 intron variant A/G snv 0.19 5
rs1800625 0.641 0.680 6 32184665 upstream gene variant A/G snv 0.15 4
rs780092 0.827 0.160 2 27520287 intron variant A/G snv 0.18 4
rs1919128 0.882 0.120 2 27578892 missense variant A/G snv 0.30 0.24 3
rs2070959 0.742 0.320 2 233693545 missense variant A/G snv 0.31 0.30 3