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
rs10069690 0.595 0.560 5 1279675 intron variant C/T snv 0.36 16
rs8170 0.724 0.160 19 17278895 synonymous variant G/A snv 0.15 0.18 3