RS115230894 CASR

Health Risk Chr 3:122282135
Upload your DNA to see your genotype for this variant.
Associated Conditions
Autosomal dominant hypocalcemia 1
Familial hypocalciuric hypercalcemia 1
Familial hypoparathyroidism
Neonatal severe primary hyperparathyroidism
Familial hypocalciuric hypercalcemia
Epilepsy
idiopathic generalized
susceptibility to
8
Hereditary cancer-predisposing syndrome
Nephrolithiasis/nephrocalcinosis
Autosomal dominant hypocalcemia 1
Familial hypocalciuric hypercalcemia 1
Familial hypoparathyroidism
Neonatal severe primary hyperparathyroidism
GWAS Studies (1)
Trait Risk Allele OR / Beta P-value Study
Serum phosphate levels — OR: 0.2 4E-14 PubMed
Other Variants in CASR
rs121909258 rs121909259 rs104893689 rs121909260 rs28936684 rs104893690 rs869320729 rs121909261 rs104893691 rs104893694
Ask Dr. Hemsworth about this variant