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: rs1057520029
rs1057520029
FGFR2
4 0.925 0.120 10 121488003 missense variant T/A snv 0.010 1.000 1 2013 2013