RS886037637 TCF12
Upload your DNA to see your genotype for this variant.
What This Variant Does
"CLNSIG=5
Associated Conditions
TCF12-related craniosynostosis
HYPOGONADOTROPIC HYPOGONADISM 26 WITH ANOSMIA
TCF12-related disorder
TCF12-related craniosynostosis
HYPOGONADOTROPIC HYPOGONADISM 26 WITH ANOSMIA
TCF12-related disorder
Other Variants in TCF12