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
rs10741657 0.637 0.520 11 14893332 upstream gene variant A/G snv 0.65 34
rs10754558 0.695 0.480 1 247448734 3 prime UTR variant G/C;T snv 20
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
rs10757283 0.827 0.120 9 22134173 intergenic variant C/A;T snv 0.45 6
rs10767664 0.752 0.400 11 27704439 intron variant T/A snv 0.83 16
rs10811661 0.724 0.400 9 22134095 intergenic variant T/C snv 0.14 22
rs10911021 0.807 0.160 1 182112825 intron variant C/T snv 0.36 11
rs11536889 0.658 0.560 9 117715853 3 prime UTR variant G/C snv 0.11 27
rs1181860747 0.776 0.240 19 7122961 missense variant C/T snv 10
rs12050217 0.827 0.160 14 96262416 intron variant A/G snv 0.21 6
rs1223493898 0.851 0.120 20 44406090 missense variant G/A;C snv 5
rs12785878 0.677 0.520 11 71456403 intron variant G/A;T snv 25
rs1282382243 0.807 0.120 13 50843630 missense variant G/A snv 8
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
rs16147 0.695 0.400 7 24283791 upstream gene variant T/C snv 0.48 18
rs16933090 0.790 0.160 11 16434247 5 prime UTR variant C/T snv 0.12 7
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
rs1799964 0.608 0.760 6 31574531 upstream gene variant T/C snv 0.19 47