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: rs7895676
rs7895676
FGFR2
2 0.925 0.080 10 121574483 intron variant C/T snv 0.40 0.010 < 0.001 1 2009 2009