Source: ALL
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: rs1354205157
rs1354205157
FGFR2
2 0.925 0.080 10 121565633 missense variant G/A snv 4.0E-06 7.0E-06 0.010 1.000 1 2012 2012
dbSNP: rs1490997619
rs1490997619
FGFR2
2 0.925 0.080 10 121488065 missense variant T/C snv 4.0E-06 0.010 1.000 1 2005 2005
dbSNP: rs751047267
rs751047267
FGFR2
2 0.925 0.080 10 121496555 missense variant T/C snv 7.0E-06 0.010 1.000 1 2005 2005
dbSNP: rs780497781
rs780497781
FGFR2
2 0.925 0.080 10 121479954 missense variant C/T snv 2.4E-05 2.8E-05 0.010 1.000 1 1995 1995