RS121918505 FGFR2

Health Risk Chr 10:121520119
Upload your DNA to see your genotype for this variant.
What This Variant Does
"[OMIM:?]
Associated Conditions
Pfeiffer syndrome
Crouzon syndrome
FGFR2-related craniosynostosis
Gastric cancer
Pfeiffer syndrome
Crouzon syndrome
FGFR2-related craniosynostosis
Gastric cancer
Other Variants in FGFR2
rs121918487 rs121918489 rs121918490 rs121918488 rs121918491 rs121918492 rs121918493 rs121918494 rs79184941 rs77543610
Ask Dr. Hemsworth about this variant