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 low infection-fighting white cells (neutrophils) in adults without known cause.
is an infiltrative brain tumor from star-shaped cells (astrocytes) in adults.
is a rare illness from gut colonization producing botulinum toxin causing paralysis.
is a rare aggressive meningeal (brain covering) tumor that can spread.
is a rare inherited leukodystrophy causing progressive nerve damage in adults.
is a rare melanoma of brain and spinal cord coverings (leptomeninges).
is a cancer of fat tissue (soft tissue sarcoma) in adults.
is a cancer of the lymphatic system; types and symptoms vary.
is a rare vascular soft-tissue cancer that can recur and spread.
is a rare, aggressive soft tissue cancer with multiple mesenchymal components.
is rare, aggressive nerve sheath cancer, often linked to neurofibromatosis type 1.
is a rare, aggressive cartilage cancer of bone or soft tissues.
is a rare inherited brain disorder causing seizures, movement, and thinking problems.
is a rare, fast-growing brain-covering tumor with high recurrence risk.
is a rare adult pineal gland brain tumor causing headaches, vision problems.
is a rare, aggressive brain tumor of the pineal gland.
is a rare, aggressive soft tissue cancer arising from skeletal muscle.
is a rare inherited disorder that affects nerves, bladder, and movement.
is a life-threatening lung condition causing severe inflammation and breathing failure.
is a rare spinal cord tumor that can cause progressive symptoms.
is an aggressive adult spinal cord cancer causing rapid neurological decline.
is a rare genetic ectodermal disorder affecting skin, nails, teeth, limbs.
is a rare, often aggressive, T-cell blood cancer linked to HTLV‑1.
is a tumor with mixed embryonic tissues, benign or malignant.