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
rs56084662
FRY
0.701 0.280 13 32295727 3 prime UTR variant G/A snv 3.5E-03 17
rs543554
FRY
1.000 0.080 13 32127501 intron variant A/G;T snv 2
rs448792
FRY
1.000 0.080 13 32103287 intron variant T/A;C snv 2
rs2520698
FRY
13 32200396 intron variant C/T snv 0.46 1
rs9533282
FRY
13 32053511 intron variant G/A;C snv 1