RS77543610 FGFR2
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What This Variant Does
"[OMIM:?]
Associated Conditions
Acrocephalosyndactyly type I
FGFR2-related craniosynostosis
11 conditions
Antley-Bixler syndrome without genital anomalies or disordered steroidogenesis
FGFR2-related disorder
Pfeiffer syndrome
Acrocephalosyndactyly type I
FGFR2-related craniosynostosis
Inborn genetic diseases
Acrocephalosyndactyly type I
FGFR2-related craniosynostosis
11 conditions
Antley-Bixler syndrome without genital anomalies or disordered steroidogenesis
FGFR2-related disorder
Pfeiffer syndrome
Other Variants in FGFR2