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 rare skin condition causing itchy, firm amyloid deposits.
is an eye condition causing raised corneal nodules and blurry vision.
is an inflammatory eye condition causing a tender, red bump.
is a benign, fast-growing soft tissue lump that is not cancer.
is a rare tumor made of immature and mature nerve cells.
is an enlarged thyroid with one or more lumps (nodules).
is a rare, usually benign tumor of the sweat glands.
is a rare skin condition causing firm, waxy bumps from mucin buildup.
is a rare, usually slow-growing Hodgkin lymphoma affecting lymph nodes.
is a serious skin cancer that begins in pigment-making cells.
is a rare brain development disorder where nerve cells are misplaced.
is a rare inflammatory condition causing tender fatty nodules under the skin.
is a rare inflammatory disorder causing tender nodules in fatty tissue.
is a noncancerous enlargement of the prostate that can affect urination.
is a rare liver condition causing tiny nodules and portal hypertension.
is a benign tendon lining growth that can cause a painful lump.
is a rare mast cell skin condition causing itchy brownish nodules.
is a severe infection that rapidly destroys tissue in mouth and face.
is a language disorder causing trouble finding words despite intact understanding.
is a rare condition causing seizures, balance problems, and sudden muscle jerks.
is long-term inflammation of the uterine lining, sometimes without clear symptoms.
causes abnormal enlargement of a limb or digits without other syndromic features.
causes the body clock to drift, disrupting regular sleep and wake times.
causes low levels of several pituitary hormones from birth.