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 birth defect where one kidney develops as nonworking cysts.
is a difficult-to-treat bacterial infection resistant to several standard tuberculosis medicines.
is a fast, irregular heart rhythm caused by multiple atrial signals.
is a movement disorder causing involuntary muscle contractions in multiple body areas.
is a rare disorder causing abnormal blood vessels and low platelets.
is a rare nerve disorder causing slowly progressive muscle weakness.
is a rare bone cancer that develops in multiple areas.
is an inherited eye disorder causing gradual central vision changes.
is tuberculosis affecting multiple body sites, often causing serious illness.
is a rare kidney cancer with multiple cyst-like areas and clear cells.
is a rare kidney tumor with cysts and low cancer risk.
is a benign kidney cyst made of several fluid-filled compartments.
is a rare genetic muscle disorder causing weakness and low muscle tone.
is a rare, usually noncancerous brain tumor often linked to seizures.
is a rare genetic condition affecting the thyroid, kidneys, and digits.
is a very rare genetic condition affecting brain, kidney, and prenatal development.
is a rare, severe condition affecting brain and kidney development before birth.
is a rare inherited disorder that impairs how the body makes energy.
is a rare inherited disorder that affects how the body uses fats.
is a rare inherited disorder causing severe energy problems in newborns.
is a rare congenital condition causing harmless ring-like skin creases on limbs.
is a rare inherited disorder that affects vitamin use and metabolism.
involves symptoms some people link to low-level everyday chemical exposures.
is a rare genetic disorder causing birth differences, hypotonia, and seizures.