RS79184941 FGFR2
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What This Variant Does
"[OMIM:?]
Associated Conditions
Acrocephalosyndactyly type I
Endometrial carcinoma
FGFR2-related craniosynostosis
11 conditions
FGFR2-related disorder
Pfeiffer syndrome
Inborn genetic diseases
Neoplasm
Liver cancer
Crouzon syndrome
FGFR2-related craniosynostosis
FGFR2-related disorder
Acrocephalosyndactyly type I
Endometrial carcinoma
FGFR2-related craniosynostosis
Other Variants in FGFR2