Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
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
rs75316749 0.701 0.280 3 169043635 intergenic variant A/G snv 4.2E-02 17
rs7725218 0.708 0.280 5 1282299 intron variant G/A snv 0.38 17
rs7931342 0.689 0.360 11 69227030 intergenic variant T/G snv 0.58 17
rs12548629 0.776 0.120 8 103189173 intron variant C/T snv 0.24 10
rs7794030 0.776 0.120 7 38712494 intergenic variant A/G snv 0.23 10
rs9834244 0.776 0.120 3 151704793 intergenic variant G/A snv 6.1E-02 10