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 disorder causing progressive leg weakness and stiffness.
is an inherited nerve disorder causing progressive leg stiffness and weakness.
is an inherited nerve disorder causing leg stiffness, weakness, and walking problems.
is a hereditary nerve disorder causing progressive leg stiffness and weakness.
is a genetic nerve disorder causing progressive leg stiffness and weakness.
is a genetic nerve condition causing progressive leg stiffness (spasticity) and weakness.
is a rare inherited disorder causing progressive leg stiffness (spasticity) and weakness.
is a genetic disorder causing progressive leg stiffness and weakness (spasticity).
is an inherited condition causing progressive leg stiffness and gait problems.
is an autosomal-dominant neurodegenerative disorder causing progressive leg stiffness and weakness.
is a genetic nerve disorder causing progressive leg stiffness (spasticity) and weakness.
is a genetic nerve disorder causing progressive leg stiffness and gait difficulties.
is an inherited nerve disorder causing progressive leg stiffness (spasticity) and weakness.
is a rare inherited disorder causing progressive leg stiffness and walking difficulties.
is an inherited nerve disorder causing progressive leg weakness and stiffness (spasticity).
is a rare inherited disorder causing spine and rib malformations.
is an autosomal-dominant bone disorder causing late-onset spine and joint problems.
is a rare inherited disorder causing progressive striatal degeneration and movement problems.
is an inherited (autosomal dominant) bleeding disorder with low, poorly functioning platelets.
is an inherited clotting disorder causing dangerous blood clots in veins.
is an inherited clotting disorder causing increased risk of blood clots.
is an inherited kidney disease causing gradual scarring and chronic kidney failure.