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 sudden intestinal blood-flow loss causing severe, life-threatening abdominal pain.
is a rare retinal disorder causing sudden blind spots and flashing lights.
is a rare inherited disorder that affects energy production in cells.
is a fatty acid oxidation disorder causing low blood sugar during fasting.
is a rare inherited disorder where cystatin C amyloid damages brain vessels.
is a rare, slow-growing basal cell carcinoma variant of the skin.
is a rare, slow-growing bone cancer, usually in the shinbone (tibia).
is a rare genetic disorder with scalp defects and limb underdevelopment.
is a rare inherited disorder with amyloid protein deposits in brain.
is a hormonal disorder where adrenal glands underproduce cortisol and aldosterone.
is a disorder where the adrenal glands make too little cortisol.
is a rare genetic disorder with joint contractures and inward-turned thumbs.
is a rare inherited enzyme disorder causing recurrent stones and kidney damage.
is a noninvasive, early glandular cancer limited to the lining.
is a malignant ovarian cancer arising from gland-forming epithelial cells.
is a rare cancer starting in anal gland cells, potentially aggressive.
is a cervical cancer arising from glandular cells producing mucus.
is a cancer starting in esophageal gland cells, often near stomach.
is a cancer starting in gland cells of gallbladder and bile ducts.
is a cancer of gland-like cells in liver and intrahepatic bile ducts.
is a rare penile cancer from glandular cells, requiring prompt treatment.
is a rare malignant tumor of glandular lining cells that can spread.
is a noncancerous (benign) tumor made of glandular and fibrous tissue.
is inflammation of the pituitary gland, causing hormone deficiencies and headaches.