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: rs773197447
rs773197447
FGFR3
1 1.000 0.080 4 1807159 missense variant G/A;C snv 3.2E-05; 2.3E-05 0.010 1.000 1 2015 2015