Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs2974935 0.708 0.280 1 155212052 non coding transcript exon variant G/A;C;T snv 17
rs481519 0.708 0.280 3 27285723 intron variant C/A;T snv 17
rs56404467
FRY
0.708 0.280 13 32265853 intron variant G/A snv 1.3E-02 17
rs73110464 0.708 0.280 12 52918828 intron variant C/T snv 0.12 17
rs7725218 0.708 0.280 5 1282299 intron variant G/A snv 0.38 17