RS776587763 FGFR2

Health Risk Chr 10:121520085
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What This Variant Does
"CLNSIG=5
Associated Conditions
Pfeiffer syndrome
FGFR2-related craniosynostosis
Crouzon syndrome
FGFR2-related disorder
Pfeiffer syndrome
FGFR2-related craniosynostosis
Crouzon syndrome
FGFR2-related disorder
Other Variants in FGFR2
rs121918487 rs121918489 rs121918490 rs121918488 rs121918491 rs121918492 rs121918493 rs121918494 rs79184941 rs77543610
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