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 cancer that starts in a fallopian tube lining.
is a rare, usually benign growth in the fallopian tube lining.
is a rare cancer that starts in the fallopian tube lining.
is a rare tumor in the fallopian tube made of different tissues.
is a rare cancer that begins in the fallopian tube lining.
is a genetic syndrome causing heart defects, learning problems, and slow growth.
is an inherited tendency to develop a dangerous bulging abdominal artery.
is a rare inherited brain disorder causing post-infection episodes of brain damage.
is an inherited condition causing many colon polyps and colorectal cancer.
is an inherited disorder causing many colon polyps and high cancer risk.
is an inherited condition causing many colon polyps and high cancer risk.
is an inherited condition causing many colon polyps and higher cancer risk.
is a rare inherited disorder affecting adrenal glands, puberty, and hormone production.
is an inherited neurological disorder causing adult-onset muscle jerks and seizures.
is an inherited brain disorder causing adult-onset muscle jerks, tremor, and seizures.
is an inherited disorder causing adult-onset muscle jerks and seizures.
is a rare inherited epilepsy causing muscle jerks and seizures in adulthood.
is a rare inherited epilepsy causing myoclonic jerks and seizures in adults.
is a rare inherited epilepsy causing adult-onset muscle jerks and seizures.
is an inherited epilepsy causing adult-onset muscle jerks and seizures.
is an inherited condition causing unusually early sleep and wake times.
is an inherited bleeding disorder caused by missing fibrinogen.
is a rare inherited prion disease causing Alzheimer-like dementia symptoms.