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: rs2162540
rs2162540
FGFR2
2 0.925 0.040 10 121592622 intron variant C/T snv 0.57 0.010 1.000 1 2019 2019