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: rs1057519038
rs1057519038
FGFR2
3 0.882 0.120 10 121520076 missense variant T/C snv 0.010 1.000 1 2002 2002