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 nerve disease causing progressive distal weakness and numbness.
is a rare inherited neuropathy causing progressive weakness and sensory problems.
is an inherited peripheral neuropathy causing progressive weakness, numbness, and foot deformities.
is a rare inherited peripheral nerve disorder causing early-onset weakness and numbness.
is a rare inherited nerve disorder causing progressive limb weakness and numbness.
is an inherited nerve disorder causing progressive weakness, numbness, and foot problems.
is a rare inherited demyelinating neuropathy causing progressive weakness and sensation loss.
is a rare inherited nerve disorder causing progressive weakness and sensation loss.
is a rare inherited nerve disorder causing early progressive weakness and numbness.
is an inherited nerve disorder causing progressive weakness and sensory loss.
is a rare inherited peripheral neuropathy causing progressive weakness and sensory loss.
is a rare inherited neuropathy causing progressive limb weakness and sensory loss.
is a rare inherited neuropathy causing progressive weakness, numbness, and deformities.
is a rare inherited nerve disorder causing muscle weakness and sensory loss.
is an inherited nerve disorder causing progressive limb weakness and sensory loss.
is a hereditary neuropathy causing limb weakness, sensory loss, and vision loss.
is a rare inherited disorder causing nerve damage, hearing loss, intellectual disability.
is a hereditary nerve disease (neuropathy) causing progressive limb weakness and numbness.
is an inherited nerve disorder causing progressive weakness, numbness, and foot changes.
is a rare genetic condition affecting multiple organs and senses from birth.
is a rare inherited nerve disorder causing ataxia and muscle stiffness (spasticity).
is a rare genetic condition affecting development and multiple body systems.
is a genetic condition affecting development, speech, learning, vision, and facial features.