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 genetic condition affecting brain development, movement, and learning.
is a rare inherited brain disorder affecting movement and development from birth.
is a rare genetic brain disorder affecting movement, development, and survival.
is a rare genetic brain disorder affecting development, movement, and coordination.
is a rare inherited brain disorder affecting development, movement, and learning.
is a rare genetic condition affecting early brain development and movement.
is a rare inherited disorder affecting brain development, movement, and breathing.
is a rare inherited disorder affecting brain development, movement, and survival.
is a rare genetic disorder affecting brain development, movement, and survival.
is a rare inherited brain disorder affecting cerebellum and brainstem development.
is a rare genetic brain-development disorder causing severe early developmental impairment.
is a rare genetic disorder affecting brain development, movement, and early growth.
is a rare inherited brain-development disorder of the pons and cerebellum.
is a rare inherited brain disorder causing severe developmental and movement problems.
is a rare genetic brain disorder causing severe developmental and movement problems.
is a rare inherited disorder affecting brain development, movement, and growth.
is a rare genetic brain disorder with underdeveloped cerebellum and brainstem.
is a rare, aggressive cancer that starts in the thymus gland.
is a rare genetic condition causing skin webs, clefts, and limb anomalies.
is a rare brain condition causing fluid-filled cavities and varied symptoms.
is a rare genetic disorder causing brain abnormalities and other birth defects.