RS121918507 FGFR2

Health Risk Chr 10:121498591
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What This Variant Does
"[OMIM:?]
Associated Conditions
Crouzon syndrome
Familial scaphocephaly syndrome
McGillivray type
Pfeiffer syndrome
FGFR2-related craniosynostosis
Crouzon syndrome
Familial scaphocephaly syndrome
McGillivray type
Pfeiffer syndrome
FGFR2-related craniosynostosis
Other Variants in FGFR2
rs121918487 rs121918489 rs121918490 rs121918488 rs121918491 rs121918492 rs121918493 rs121918494 rs79184941 rs77543610
Ask Dr. Hemsworth about this variant