RS121918491 FGFR2

Health Risk Chr 10:121517371
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What This Variant Does
"[OMIM:?]
Associated Conditions
SCAPHOCEPHALY AND AXENFELD-RIEGER ANOMALY
Crouzon syndrome
CRANIOSYNOSTOSIS
NONCLASSIFIABLE AUTOSOMAL DOMINANT
Craniosynostosis syndrome
FGFR2-related craniosynostosis
11 conditions
Acrocephalosyndactyly type I
FGFR2-related disorder
Common craniosynostosis syndromes
Hepatocellular carcinoma
SCAPHOCEPHALY AND AXENFELD-RIEGER ANOMALY
Crouzon syndrome
CRANIOSYNOSTOSIS
NONCLASSIFIABLE AUTOSOMAL DOMINANT
Other Variants in FGFR2
rs121918487 rs121918489 rs121918490 rs121918488 rs121918492 rs121918493 rs121918494 rs79184941 rs77543610 rs121918495
Ask Dr. Hemsworth about this variant