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 hereditary spastic paraplegia (HSP) causing progressive leg stiffness, weakness.
is a rare inherited disorder causing leg stiffness, weakness, and gait problems.
is a rare autosomal recessive disorder causing progressive leg spasticity and weakness.
is a rare inherited nerve disorder causing progressive leg stiffness and weakness.
is a rare autosomal recessive disorder causing progressive leg stiffness and weakness.
is a rare inherited disorder causing progressive leg stiffness and walking difficulties.
is an autosomal recessive nerve disorder causing progressive leg spasticity and weakness.
is an autosomal recessive disorder causing progressive leg stiffness (spasticity) and weakness.
is a rare inherited disorder causing progressive leg stiffness and weakness (spasticity).
is an autosomal recessive neurological disorder causing progressive leg stiffness and weakness.
is a rare autosomal recessive nerve disorder causing progressive leg weakness, stiffness.
is a rare autosomal recessive disorder causing progressive leg stiffness (spasticity).
is a rare autosomal recessive nerve disorder causing progressive leg stiffness, weakness.
is an inherited nerve disorder causing progressive leg stiffness (spasticity) and weakness.
is a rare genetic condition causing progressive leg stiffness (spasticity) and weakness.
