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 inherited nerve disorder affecting pain, temperature, and sweating.
is a rare inherited disorder causing nerve damage, deafness, and developmental delay.
is an inherited nerve disorder causing reduced sensation, injuries, and sometimes weakness.
is an inherited nerve disorder causing pain, numbness, and weakness.
is an inherited nerve disorder causing worsening numbness, pain, and weakness.
is an inherited nerve disorder causing reduced pain sensation and injuries.
is an inherited nerve disorder affecting sensation, often mainly in boys.
is an inherited disorder causing sensory nerve damage (neuropathy), hearing loss, dementia.
is a group of inherited disorders causing progressive leg weakness and stiffness.
is an inherited nerve disorder causing progressive leg stiffness and weakness.
is an inherited condition causing progressive leg stiffness, weakness, and walking problems.
is a rare inherited nerve disorder causing progressive leg stiffness and weakness.
is an inherited nerve disorder causing leg stiffness, weakness, and walking problems.
is an inherited disorder causing progressive leg stiffness, weakness, and walking problems.
is a rare inherited disorder causing progressive leg stiffness and weakness.
is an inherited condition causing progressive leg stiffness and walking problems.
