RS1553766262 CASR

Health Risk Chr 3:122257279
Upload your DNA to see your genotype for this variant.
Associated Conditions
Inborn genetic diseases
Familial hypocalciuric hypercalcemia
Autosomal dominant hypocalcemia 1
Nephrolithiasis/nephrocalcinosis
Inborn genetic diseases
Familial hypocalciuric hypercalcemia
Autosomal dominant hypocalcemia 1
Nephrolithiasis/nephrocalcinosis
Other Variants in CASR
rs121909258 rs121909259 rs104893689 rs121909260 rs28936684 rs104893690 rs869320729 rs121909261 rs104893691 rs104893694
Ask Dr. Hemsworth about this variant