rs2032582 is a genetic variant on gene ABCB1 associated with Inflammatory bowel disease 13.
rs10876864 is a genetic variant on gene IKZF4 associated with Intelligence and Allergic disease.
rs11540652 is a genetic variant on gene TP53 associated with Li-fraumeni syndrome 1 and Multiple myeloma.
rs104894226 is a genetic variant on gene HRAS associated with Costello syndrome and Large congenital melanocytic nevus.
rs7274581 is a genetic variant associated with Alzheimer's disease.
rs10808546 is a genetic variant associated with Abdominal aortic aneurysm.
is abnormally low pressure inside the eye that can threaten vision.
is a rare eruption disorder causing teeth not to emerge properly.
is a rare inherited disorder that causes too many red blood cells.
is a rare inherited kidney tubule disorder causing nutrient loss in urine.
is tuberculosis affecting the kidneys, bladder, or reproductive organs.
is a rare brain or spinal cord tumor from germ cells.
is an inherited immune disorder causing severe, life-threatening inflammation.
is a rare cancer that starts in neuroendocrine cells of the liver.
is a rare inherited disorder causing excess aldosterone, seizures, and neurological problems.
is a rare blood disorder with too many eosinophils harming organs.
is a rare genetic condition causing underactive gonads and partial hair loss.
is a rare inherited disorder causing excess oxalate, kidney stones, kidney damage.
is a rare inherited liver enzyme disorder causing oxalate buildup, kidney damage.
is a rare genetic enzyme defect causing oxalate buildup and kidney stones.
is a rare inherited disorder causing excess oxalate and recurrent kidney stones.
is overactivity of parathyroid glands, raising blood calcium and affecting bones, kidneys.
is a rare genetic disorder causing clubbing, thickened skin, and joint pain.
is a rare disorder causing low magnesium levels and related symptoms.
is a rare inherited kidney disorder causing magnesium loss and calcium buildup.
is an inherited disorder causing kidney magnesium loss and serious eye problems.
is a rare inherited kidney disorder causing magnesium loss and kidney calcification.
is a rare inherited disorder causing very low magnesium and calcium levels.
is a genetic condition causing low magnesium, seizures, developmental disability, and obesity.
is a rare inherited disorder causing low magnesium, seizures, and developmental delays.