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: rs387906678
rs387906678
FGFR2
5 0.851 0.120 10 121515263 missense variant A/C;G snv 0.800 1.000 1 2012 2012