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 kidney disorder causing heavy protein loss and swelling.
is a genetic kidney disorder causing heavy protein loss in urine.
is a rare inherited kidney disorder causing heavy protein loss in urine.
is a rare genetic kidney disorder causing heavy protein loss in urine.
is an inherited kidney disorder causing severe protein loss in urine.
is a rare inherited kidney disorder causing protein loss and body swelling.
is an inherited kidney disorder causing heavy protein loss in urine.
is a rare inherited kidney disorder causing severe protein loss in urine.
is a genetic kidney disorder causing heavy protein loss and swelling.
is a kidney disorder causing heavy protein loss, swelling, and infection risk.
is a kidney disorder causing heavy protein loss and body swelling.
is a rare genetic kidney disorder causing severe protein loss in urine.
is a kidney disorder causing protein loss, swelling, and low blood protein.
is a rare inherited disorder causing kidney disease, fragile skin, and deafness.
is a condition caused by pressure on a nerve.
involves abnormal development of bundles of nerve fibers in the body.
is a tumor that grows in a network of nerves.
is a tumor growing from a spinal nerve root.
is a noncancerous tumor in the brain, spinal cord, or nerves.
is cancer that begins in the brain, spinal cord, or nerves.
