RS104893708 CASR

Health Risk Chr 3:122257269
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What This Variant Does
"[OMIM:?]
Associated Conditions
Autosomal dominant hypocalcemia 1
Bartter syndrome with hypocalcemia
Epilepsy
idiopathic generalized
susceptibility to
8
Neonatal severe primary hyperparathyroidism
Familial hypocalciuric hypercalcemia 1
Familial hypocalciuric hypercalcemia
Autosomal dominant hypocalcemia 1
Bartter syndrome with hypocalcemia
Epilepsy
idiopathic generalized
susceptibility to
8
Other Variants in CASR
rs121909258 rs121909259 rs104893689 rs121909260 rs28936684 rs104893690 rs869320729 rs121909261 rs104893691 rs104893694
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