Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs72563732 0.882 0.040 3 186854563 synonymous variant C/T snv 6.4E-05 2.6E-04 3
rs738407 1.000 0.040 22 43928075 intron variant T/A;C;G snv 1
rs2143571 0.827 0.080 22 43995806 intron variant G/A snv 0.25 5
rs17007417 0.882 0.080 2 71808541 regulatory region variant T/C snv 0.85 3
rs13412852 0.851 0.120 2 11774815 intron variant C/T snv 0.26 4
rs121909244 0.776 0.160 3 12434111 missense variant C/A;T snv 4.0E-06 11
rs2896019 0.790 0.160 22 43937814 intron variant T/G snv 0.20 10
rs694539 0.776 0.200 11 114262697 intron variant C/T snv 0.21 10
rs641738 0.689 0.320 19 54173068 missense variant T/A;C;G snv 22
rs72613567 0.742 0.320 4 87310240 splice donor variant -/A delins 0.22 14
rs780094 0.658 0.400 2 27518370 intron variant T/C snv 0.67 62
rs58542926 0.630 0.440 19 19268740 missense variant C/T snv 6.5E-02 5.8E-02 42
rs1260326 0.645 0.600 2 27508073 missense variant T/C;G snv 0.63; 4.0E-06 0.68 81
rs1800206 0.641 0.640 22 46218377 missense variant C/G snv 4.3E-02 4.2E-02 35
rs738409 0.557 0.720 22 43928847 missense variant C/G snv 0.28 0.22 88
rs1799945 0.452 0.760 6 26090951 missense variant C/G;T snv 0.11 0.10 226
rs1800562 0.435 0.880 6 26092913 missense variant G/A snv 3.3E-02 3.8E-02 262