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 a chronic sleep disorder causing sudden sleepiness and cataplexy.
is a sleep disorder causing excessive daytime sleepiness without cataplexy.
is a rare inherited mitochondrial disorder affecting nerves, muscles, vision, and development.
is a rare cancer that starts in the lining of the nose.
is a noncancerous growth in the inside of the nose.
is a rare cancer that starts in the tissues inside the nose.
is an early-stage cancer limited to the nasal cavity lining.
affects the inside of the nose, causing breathing problems and discomfort.
is a usually benign nasal tumor that can return or become cancerous.
is a rare cancer that starts in tissues inside the nose.
is a rare cancer that starts in smell nerve tissue.
is a birth defect causing a cyst or tract on the nose.
is a rare tunnel-like opening along the bridge of the nose.
is a rare birth defect where brain tissue protrudes through the nose.
is a rare, usually benign tumor of nerve and support cells.
is a rare, noncancerous birth defect with brain tissue near the nose.
is a rare, aggressive lymphoma that often starts in the nose.
is a usually benign wart-like growth inside the front of the nose.
is a fluid-filled blockage near the tear duct, often in newborns.
is a rare genetic condition affecting eyelid development and facial tissues.
is a throat cancer behind the nose, often linked to Epstein‑Barr virus.
is a condition affecting the upper throat behind the nose.