RS764959117 FGFR2

Health Risk Chr 10:121479907
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Associated Conditions
Craniosynostosis syndrome
Beare-Stevenson cutis gyrata syndrome
Crouzon syndrome
Saethre-Chotzen syndrome
Isolated Coronal Synostosis
FGFR2-related craniosynostosis
Inborn genetic diseases
Craniosynostosis syndrome
Beare-Stevenson cutis gyrata syndrome
Crouzon syndrome
Saethre-Chotzen syndrome
Isolated Coronal Synostosis
FGFR2-related craniosynostosis
Inborn genetic diseases
Other Variants in FGFR2
rs121918487 rs121918489 rs121918490 rs121918488 rs121918491 rs121918492 rs121918493 rs121918494 rs79184941 rs77543610
Ask Dr. Hemsworth about this variant