Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs10455872
LPA
0.662 0.320 6 160589086 intron variant A/G snv 4.3E-02 33
rs10757274 0.701 0.320 9 22096056 intron variant A/G snv 0.41 22
rs10757278 0.620 0.520 9 22124478 intron variant A/G snv 0.40 44
rs10767664 0.752 0.400 11 27704439 intron variant T/A snv 0.83 16
rs10911021 0.807 0.160 1 182112825 intron variant C/T snv 0.36 11
rs12050217 0.827 0.160 14 96262416 intron variant A/G snv 0.21 6
rs12785878 0.677 0.520 11 71456403 intron variant G/A;T snv 25
rs12979860 0.547 0.520 19 39248147 intron variant C/T snv 0.39 84
rs1333049 0.614 0.520 9 22125504 intron variant G/C snv 0.41 60
rs1408888 0.851 0.120 13 71854515 intron variant T/G snv 0.30 5
rs1467568 0.776 0.320 10 67915401 intron variant A/G snv 0.46 8
rs1501299 0.597 0.720 3 186853334 intron variant G/C;T snv 52
rs17251221 0.724 0.360 3 122274400 intron variant A/G snv 0.11 18
rs1799750 0.592 0.760 11 102799765 intron variant C/- delins 0.50 48
rs1800795 0.494 0.840 7 22727026 intron variant C/G snv 0.71 140
rs182052 0.701 0.440 3 186842993 intron variant G/A snv 0.38 19
rs184003 0.724 0.400 6 32182519 intron variant C/A snv 0.12 0.12 15
rs2282679
GC
0.645 0.480 4 71742666 intron variant T/G snv 0.21 38
rs2383207 0.695 0.280 9 22115960 intron variant A/G snv 0.64 22
rs2518136 0.851 0.120 3 186620038 intron variant T/C snv 0.46 4
rs4977574 0.695 0.520 9 22098575 intron variant A/G;T snv 26
rs6700896 0.827 0.160 1 65624099 intron variant C/T snv 0.44 9
rs6721961 0.672 0.520 2 177265309 intron variant T/C;G snv 0.89 24
rs708272 0.708 0.440 16 56962376 intron variant G/A snv 0.42 0.38 24
rs7903146 0.554 0.680 10 112998590 intron variant C/G;T snv 93