RS566155088 FGFR2

Health Risk Chr 10:121479183
Upload your DNA to see your genotype for this variant.
Associated Conditions
Beare-Stevenson cutis gyrata syndrome
Isolated Coronal Synostosis
Crouzon syndrome
Craniosynostosis syndrome
Saethre-Chotzen syndrome
Beare-Stevenson cutis gyrata syndrome
Isolated Coronal Synostosis
Crouzon syndrome
Craniosynostosis syndrome
Saethre-Chotzen syndrome
Other Variants in FGFR2
rs121918487 rs121918489 rs121918490 rs121918488 rs121918491 rs121918492 rs121918493 rs121918494 rs79184941 rs77543610
Ask Dr. Hemsworth about this variant