Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs104886003 0.562 0.440 3 179218303 missense variant G/A;C snv 4.0E-06 35
rs671 0.529 0.840 12 111803962 missense variant G/A snv 1.9E-02 5.8E-03 29
rs1229984 0.570 0.560 4 99318162 missense variant T/C;G snv 0.90 27
rs121913273 0.605 0.440 3 179218294 missense variant G/A;C snv 25
rs2075650 0.662 0.360 19 44892362 intron variant A/G snv 0.13 0.13 25
rs7412 0.641 0.640 19 44908822 missense variant C/T snv 6.2E-02 7.9E-02 23
rs121913483 0.649 0.560 4 1801841 missense variant C/A;G;T snv 4.2E-06; 1.3E-05 23
rs12203592 0.649 0.320 6 396321 intron variant C/T snv 0.10 23
rs4803750 0.807 0.240 19 44744370 upstream gene variant A/G snv 7.7E-02 22
rs113488022 0.351 0.840 7 140753336 missense variant A/C;G;T snv 4.0E-06 22
rs11571833 0.608 0.360 13 32398489 stop gained A/T snv 6.6E-03 6.0E-03 21
rs1126809 0.683 0.320 11 89284793 missense variant G/A snv 0.18 0.18 20
rs72928038 0.695 0.360 6 90267049 intron variant G/A snv 0.11 19
rs401681 0.620 0.640 5 1321972 intron variant C/T snv 0.48 17
rs1805007 0.695 0.280 16 89919709 missense variant C/A;G;T snv 4.4E-02 16
rs2736100 0.550 0.880 5 1286401 3 prime UTR variant C/A snv 0.52 16
rs646776 0.752 0.240 1 109275908 downstream gene variant C/T snv 0.74 15
rs17879961 0.597 0.480 22 28725099 missense variant A/C;G snv 4.1E-03 15
rs602662 0.716 0.280 19 48703728 missense variant G/A snv 0.40 0.47 15
rs12916300 0.742 0.080 15 28165345 intron variant C/T snv 0.50 13
rs121913530 0.583 0.640 12 25245351 missense variant C/A;G;T snv 13
rs6511720 0.790 0.120 19 11091630 intron variant G/T snv 0.12 13
rs10455872
LPA
0.662 0.320 6 160589086 intron variant A/G snv 4.3E-02 12
rs587782289 0.752 0.240 17 7674257 missense variant A/C;G;T snv 12
rs1051730 0.641 0.600 15 78601997 synonymous variant G/A snv 0.27 0.26 11