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 an inherited brain disorder causing progressive coordination and balance problems.
is a rare inherited disorder causing balance problems, hearing loss, and narcolepsy.
is an autosomal dominant disorder causing balance (ataxia), hearing loss, narcolepsy.
is an autosomal dominant neuropathy causing progressive distal weakness and numbness.
is a rare autosomal dominant neuropathy causing progressive distal weakness and numbness.
is an inherited nerve disorder causing progressive weakness, numbness, and foot problems.
is a hereditary nerve disorder (peripheral neuropathy) causing progressive limb weakness.
is an autosomal-dominant peripheral neuropathy with giant axons causing distal weakness.
is an inherited nerve disorder causing progressive weakness and numbness in limbs.
is a genetic peripheral neuropathy causing progressive distal weakness and numbness.
is a hereditary nerve disorder causing progressive weakness and sensory loss.
is a hereditary nerve disorder (peripheral neuropathy) causing hand and foot weakness.
is a hereditary axonal neuropathy causing progressive distal weakness and numbness.
is an inherited peripheral neuropathy causing progressive hand and foot weakness, numbness.
is an inherited peripheral nerve disorder (neuropathy) causing progressive weakness and numbness.
is a genetic nerve disorder causing progressive weakness, wasting, and sensory loss.
is a hereditary peripheral nerve disorder causing progressive distal weakness and numbness.
is a hereditary peripheral neuropathy causing progressive distal weakness and sensory loss.
is an autosomal-dominant peripheral nerve disorder causing progressive limb weakness and numbness.
is an autosomal dominant nerve disease (neuropathy) causing progressive distal weakness, numbness.
is a hereditary nerve disorder (neuropathy) causing progressive distal weakness, numbness.
is a genetic peripheral neuropathy causing progressive weakness and numbness in limbs.
