Variant Gene N. diseases v DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Score vda EI vda N. PMIDs First Ref. Last Ref.
dbSNP: rs2066854
rs2066854
FGG
1 4 154614029 upstream gene variant T/A snv 0.25 0.700 1.000 1 2012 2012
dbSNP: rs2066861
rs2066861
FGG
5 4 154606284 intron variant C/T snv 0.26 0.700 1.000 1 2012 2012
dbSNP: rs2066864
rs2066864
FGG
2 4 154604543 3 prime UTR variant G/A snv 0.26 0.700 1.000 1 2012 2012
dbSNP: rs2066865
rs2066865
FGG
10 0.807 0.240 4 154604124 downstream gene variant G/A snv 0.26 0.700 1.000 1 2012 2012