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 autosomal recessive disease causing early progressive cerebellar ataxia.
is a rare autosomal recessive ataxia causing progressive coordination and balance problems.
is a rare inherited nerve disorder causing progressive balance and coordination problems.
is a rare inherited disorder causing progressive balance and coordination problems.
is a rare genetic ataxia causing progressive balance, coordination, and speech problems.
is a rare autosomal recessive disorder causing progressive balance and coordination difficulties.
is a rare inherited disorder causing early-onset cerebellar ataxia and developmental delay.
is a rare inherited disorder causing progressive balance, coordination, and speech problems.
is a rare autosomal recessive neurologic disorder causing progressive ataxia.
is a rare inherited neurological disorder causing progressive coordination and balance problems.
is a rare inherited disorder causing progressive coordination, balance, and speech problems.
is an autosomal-recessive disorder causing coordination problems (ataxia) and slurred speech (dysarthria).
is an autosomal recessive disorder causing progressive balance and coordination difficulties.
is a rare autosomal recessive cerebellar disorder causing coordination and balance problems.
is a rare autosomal recessive disorder causing progressive balance problems (ataxia).
is a rare inherited disorder causing progressive coordination and balance problems.
is a rare inherited neurologic disorder causing progressive ataxia and coordination difficulties.
is a rare genetic disorder causing progressive balance and coordination (ataxia) problems.
is a rare autosomal recessive disorder causing progressive balance and coordination problems.
is a rare inherited disorder causing coordination loss, vision and hearing impairment.
is a rare inherited disorder causing abnormal spine and rib development.
is a rare autosomal recessive bone disorder affecting spine and joints.
is a rare genetic bone disorder causing short stature and joint problems.
is a rare inherited bone growth disorder affecting spine and limb bones.