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 movement disorder causing involuntary muscle contractions on one side.
is a rare movement disorder causing one-sided twisting and body wasting.
is a rare condition causing overgrowth on one side of the face.
causes one side of the face muscles to grow larger.
is a nerve-related condition causing repeated, involuntary twitching on one side.
is a rare overgrowth disorder causing body asymmetry and multiple fatty lumps.
is a rare brain difference where one side grows abnormally large.
is a rare birth difference where part of a limb is missing.
is a rare disorder causing one-sided body wasting and Parkinson-like symptoms.
is paralysis or severe weakness on one side of the body.
is a disorder causing iron overload, usually inherited, damaging organs.
is an inherited disorder causing severe iron buildup, often starting young.
is a rare genetic condition causing early, severe iron overload.
is an inherited iron overload disorder that can damage organs over time.
is an inherited blood disorder that can cause mild anemia.
is an inherited blood disorder causing anemia from abnormal hemoglobin production.
is an inherited hemoglobin variant affecting red blood cells, usually mild.
is an inherited hemoglobin condition causing mild anemia, common in Southeast Asians.
is an inherited blood disorder causing variable anemia and hemoglobin imbalance.
is an inherited blood disorder that can cause lifelong anemia.
is an inherited blood disorder that can cause mild to severe anemia.
is a rare inherited condition causing abnormal hemoglobin and bluish skin color.
is an inherited blood disorder affecting hemoglobin, the protein that carries oxygen.
is a rare inherited hemoglobin disorder that affects red blood cells.