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 testicular cancer that develops in a testicle that never descended.
is a rare cancer of the thymus, a gland behind the breastbone.
is a rare cancer of the thymus that can spread nearby.
is a rare cancer affecting the lining around the lungs.
is a rare inherited disorder that affects energy production.
is a birth defect where a coronary artery starts abnormally.
is a slow-growing cancer of immune tissue, often starting in the stomach.
is a type of hypersensitivity pneumonitis caused by inhaling moldy malt dust.
is a rare salivary gland cancer that often grows slowly.
is a rare breast cancer of the nipple and areola skin.
is a rare genetic condition affecting the breasts, fingers, and nails.
is a rare inherited disorder affecting protein processing, development, and growth.
is an abnormal tangle of blood vessels in the lower jaw.
is a rare cancer that starts in the lower jawbone.
is a rare genetic condition causing small jaw, deafness, and fat loss.
is a rare inherited disorder affecting bone development, growth, and skin.
is a rare genetic disorder affecting bone development, skin, and growth.
is a rare inherited disorder affecting body fat, bones, and growth.
is a rare genetic disorder causing bone changes and partial fat loss.
is a rare inherited disorder affecting bones, skin, and body fat.
is a rare genetic condition affecting facial bone development and sometimes hearing.
is a rare genetic disorder affecting facial bones, scalp hair, and hearing.
is a rare genetic condition affecting facial development, eyelids, and mouth size.
is a rare condition causing small head, facial differences, and developmental delay.