RS121918488 FGFR2
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What This Variant Does
"[OMIM:?]
Associated Conditions
Pfeiffer syndrome
Antley-Bixler syndrome without genital anomalies or disordered steroidogenesis
Crouzon syndrome
Jackson-Weiss syndrome
FGFR2-related craniosynostosis
Crouzon syndrome
Jackson-Weiss syndrome
Antley-Bixler syndrome without genital anomalies or disordered steroidogenesis
Pfeiffer syndrome
FGFR2-related craniosynostosis
Pfeiffer syndrome
FGFR2-related syndromic and non-syndromic craniosynostoses
FGFR2-related craniosynostosis
Pfeiffer syndrome
Antley-Bixler syndrome without genital anomalies or disordered steroidogenesis
Other Variants in FGFR2