RS104893697 CASR

Health Risk Chr 3:122261606
Upload your DNA to see your genotype for this variant.
What This Variant Does
"[OMIM:?]
Associated Conditions
Autosomal dominant hypocalcemia 1
Epilepsy
idiopathic generalized
susceptibility to
8
Neonatal severe primary hyperparathyroidism
Familial hypocalciuric hypercalcemia 1
Autosomal dominant hypocalcemia 1
Epilepsy
idiopathic generalized
susceptibility to
8
Neonatal severe primary hyperparathyroidism
Familial hypocalciuric hypercalcemia 1
Other Variants in CASR
rs121909258 rs121909259 rs104893689 rs121909260 rs28936684 rs104893690 rs869320729 rs121909261 rs104893691 rs104893694
Ask Dr. Hemsworth about this variant