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: rs1800791
rs1800791
FGB
1 1.000 0.080 4 154562157 upstream gene variant G/A snv 0.15 0.010 1.000 1 2006 2006
dbSNP: rs749785846
rs749785846
FGB
2 0.925 0.160 4 154568469 synonymous variant C/T snv 4.0E-06 0.010 1.000 1 2003 2003
dbSNP: rs761740955
rs761740955
FGB
5 0.827 0.200 4 154566637 missense variant A/G snv 4.0E-06 0.010 1.000 1 2009 2009