Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs2228145 0.602 0.720 1 154454494 missense variant A/C;T snv 0.38; 1.2E-05 5
rs4129267 0.807 0.200 1 154453788 intron variant C/G;T snv 5
rs7529229 0.851 0.120 1 154448302 intron variant T/C snv 0.48 4
rs4537545 0.790 0.160 1 154446403 intron variant C/T snv 0.48 4
rs7518199 1 154434943 intron variant A/C;T snv 0.39; 4.2E-06 4
rs4845625 0.851 0.080 1 154449591 intron variant T/C snv 0.60 3
rs12089132 1 154405860 intron variant T/C snv 1.2E-02 2
rs1552481 1 154403877 non coding transcript exon variant C/T snv 0.94 2
rs2229238 0.851 0.080 1 154465420 3 prime UTR variant T/A;C snv 0.80 1
rs28638007 1 154448878 intron variant T/C snv 9.3E-02 1
rs4845618 0.851 0.160 1 154427539 intron variant G/T snv 0.53 1