Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs780094 0.658 0.400 2 27518370 intron variant T/C snv 0.67 62
rs3918242 0.602 0.680 20 46007337 upstream gene variant C/T snv 0.14 54
rs174547 0.742 0.240 11 61803311 intron variant T/C snv 0.28 33
rs662799 0.689 0.480 11 116792991 upstream gene variant G/A snv 0.90 33
rs17577 0.649 0.520 20 46014472 missense variant G/A;C snv 0.16 31
rs780093 0.763 0.240 2 27519736 intron variant T/C snv 0.68 30
rs579459 0.752 0.320 9 133278724 upstream gene variant C/T snv 0.81 28
rs599839 0.724 0.360 1 109279544 downstream gene variant G/A;C snv 27
rs646776 0.752 0.240 1 109275908 downstream gene variant C/T snv 0.74 25
rs495828 0.827 0.200 9 133279294 upstream gene variant T/G snv 0.81 24
rs693 0.708 0.440 2 21009323 synonymous variant G/A snv 0.39 0.38 24
rs708272 0.708 0.440 16 56962376 intron variant G/A snv 0.42 0.38 24
rs174537 0.708 0.400 11 61785208 non coding transcript exon variant G/T snv 0.28 23
rs657152
ABO
0.882 0.200 9 133263862 intron variant A/C;T snv 22
rs2108622 0.742 0.280 19 15879621 missense variant C/T snv 0.27 0.22 20
rs2266788 0.763 0.440 11 116789970 3 prime UTR variant G/A snv 0.93 19
rs328
LPL
0.732 0.440 8 19962213 stop gained C/G snv 9.2E-02 9.0E-02 19
rs1800775 0.790 0.240 16 56961324 upstream gene variant C/A;G snv 0.51; 5.7E-06 18
rs887829 0.763 0.280 2 233759924 intron variant C/T snv 0.36 18
rs174546 0.807 0.200 11 61802358 3 prime UTR variant C/T snv 0.28 17
rs11206510 0.763 0.240 1 55030366 intergenic variant T/A;C;G snv 16
rs12740374 0.851 0.040 1 109274968 3 prime UTR variant G/T snv 0.22 16
rs1800588 0.790 0.200 15 58431476 intron variant C/G;T snv 0.30 16
rs6511720 0.790 0.120 19 11091630 intron variant G/T snv 0.12 15
rs2228671 0.790 0.160 19 11100236 stop gained C/A;G;T snv 1.6E-05; 8.9E-02 14