Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs17235409 0.653 0.600 2 218395009 missense variant G/A;C snv 4.9E-02; 4.1E-06 31
rs17235416 0.807 0.200 2 218395091 3 prime UTR variant TGTG/- del 8.4E-02 6
rs3731865 0.882 0.160 2 218385280 non coding transcript exon variant G/A;C;T snv 0.23; 1.4E-04 5
rs201565523 0.925 0.240 2 218390027 missense variant C/T snv 2.9E-04 7.7E-05 3
rs34448891 0.925 0.160 2 218381927 upstream gene variant TGTGTGTG/-;TG;TGTG;TGTGTG;TGTGTGTGTG;TGTGTGTGTGTG;TGTGTGTGTGTGTG;TGTGTGTGTGTGTGTG delins 2
rs3731863 0.925 0.040 2 218387485 intron variant C/T snv 8.0E-02 2
rs751683612 1.000 0.040 2 218394932 missense variant C/T snv 4.0E-06 7.0E-06 1