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 disorder affecting brain myelin, movement, and development.
is a rare genetic disorder that affects myelin, movement, and development.
is a rare genetic disorder affecting myelin, movement, development, and learning.
is a rare inherited disorder affecting myelin, movement, development, and speech.
is a rare inherited disorder affecting brain white matter and movement.
is a rare inherited disorder affecting myelin, movement, coordination, and development.
is a rare genetic disorder causing poor myelin, movement imbalance, missing teeth.
is a rare genetic brain disorder affecting myelin, movement, and development.
is a rare genetic disorder causing poor nerve myelination and joint contractures.
is a rare genetic brain disorder with low myelin and movement problems.
is a rare inherited disorder affecting myelin, movement, and coordination.
is a rare genetic brain disorder affecting myelin, balance, and development.
is a rare genetic disorder affecting brain myelin and causing cataracts.
is a rare genetic disorder affecting brain myelin, puberty, and tooth development.
is a genetic disorder causing low calcium, hearing loss, and kidney problems.
is a rare throat cancer that starts in the lower throat.