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 bladder cancer classified by how deeply it has grown.
is a rare genetic condition affecting the pancreas, growth, development, and appearance.
is a rare genetic condition affecting the skin, hair, teeth, and nails.
are birth differences affecting how joints develop, align, and move.
is a rare genetic disorder affecting brain development, coordination, and breathing.
is a rare inherited brain disorder causing developmental delay and coordination problems.
is a rare genetic brain disorder affecting development, movement, and breathing.
is a rare genetic condition affecting brain development and coordination.
is a rare inherited disorder affecting brain development and body systems.
is a rare genetic ciliopathy causing developmental delay and cerebellar abnormalities.
is a rare genetic condition affecting brain development, movement, and breathing.
is a rare inherited brain-development disorder with variable symptoms and severity.
is a rare genetic brain disorder causing developmental delays and coordination problems.
is a rare genetic disorder affecting brain development, movement, breathing, and vision.
is a rare inherited brain-development disorder causing coordination, breathing, and developmental problems.
is a rare inherited brain-development disorder causing coordination, breathing, and vision problems.
is a rare inherited brain development disorder affecting movement, breathing, and development.
is a rare inherited disorder affecting brain development, movement, and coordination.
is a rare inherited ciliopathy (cilia-related disorder) affecting brain development and breathing.
is a rare genetic condition that affects brain development and body control.
is a rare genetic brain disorder affecting development, movement, and coordination.