Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs2066861
FGG
4 154606284 intron variant C/T snv 0.26 5
rs6050
FGA
0.827 0.120 4 154586438 missense variant T/A;C snv 0.29 5
rs7681423 4 154621096 intergenic variant C/T snv 0.26 5