Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs3184504 0.572 0.600 12 111446804 missense variant T/A;C;G snv 0.67 61
rs1260326 0.645 0.600 2 27508073 missense variant T/C;G snv 0.63; 4.0E-06 0.68 55
rs780094 0.658 0.400 2 27518370 intron variant T/C snv 0.67 35
rs964184 0.716 0.440 11 116778201 3 prime UTR variant G/C snv 0.82 35
rs4420638 0.708 0.520 19 44919689 downstream gene variant A/G snv 0.18 30
rs429358 0.590 0.600 19 44908684 missense variant T/C snv 0.14 0.16 26
rs653178 0.672 0.600 12 111569952 intron variant C/T snv 0.67 23
rs79105258 12 111280427 intron variant C/A;T snv 23
rs10401969 0.776 0.240 19 19296909 intron variant T/C snv 0.10 22
rs7412 0.641 0.640 19 44908822 missense variant C/T snv 6.2E-02 7.9E-02 20
rs174547 0.742 0.240 11 61803311 intron variant T/C snv 0.28 20
rs4803750 0.807 0.240 19 44744370 upstream gene variant A/G snv 7.7E-02 19
rs629301 0.851 0.120 1 109275684 3 prime UTR variant G/T snv 0.74 19
rs247617 0.827 0.160 16 56956804 regulatory region variant C/A snv 0.29 18
rs1535 0.752 0.240 11 61830500 intron variant A/G snv 0.31 18
rs1800562 0.435 0.880 6 26092913 missense variant G/A snv 3.3E-02 3.8E-02 18
rs562338 0.807 0.160 2 21065449 intergenic variant A/G snv 0.69 17
rs635634 0.882 0.160 9 133279427 upstream gene variant T/A;C snv 17
rs7703051 0.851 0.120 5 75329662 intron variant C/A snv 0.38 17
rs1800961 0.851 0.160 20 44413724 missense variant C/T snv 3.1E-02 2.5E-02 17
rs174533 0.763 0.160 11 61781553 intron variant G/A snv 0.37 0.29 17
rs28929474 0.708 0.320 14 94378610 missense variant C/G;T snv 2.8E-05; 1.1E-02 17
rs855791 0.701 0.400 22 37066896 missense variant A/G;T snv 0.57; 4.0E-06 17
rs478442 0.851 0.120 2 21176344 intergenic variant G/C;T snv 16
rs780093 0.763 0.240 2 27519736 intron variant T/C snv 0.68 16