RS121909266 CASR

Health Risk Chr 3:122257091
Upload your DNA to see your genotype for this variant.
What This Variant Does
"[OMIM:?]
Associated Conditions
Familial hypocalciuric hypercalcemia 1
Autosomal dominant hypocalcemia 1
Familial hypocalciuric hypercalcemia
Neonatal severe primary hyperparathyroidism
Epilepsy
idiopathic generalized
susceptibility to
8
Familial hypocalciuric hypercalcemia 1
Autosomal dominant hypocalcemia 1
Familial hypocalciuric hypercalcemia
Neonatal severe primary hyperparathyroidism
Epilepsy
idiopathic generalized
susceptibility to
Other Variants in CASR
rs121909258 rs121909259 rs104893689 rs121909260 rs28936684 rs104893690 rs869320729 rs121909261 rs104893691 rs104893694
Ask Dr. Hemsworth about this variant