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 anemia that reduces red blood cell production.
is a rare inherited disorder that reduces red blood cell production.
is a rare inherited disorder causing anemia and distinctive facial differences.
is a rare inherited condition causing anemia and distinctive facial differences.
is a rare inherited disorder that causes anemia and other birth differences.
is an inherited disorder that reduces red blood cell production.
is a rare inherited disorder causing low red blood cells and anemia.
is a rare inherited bone marrow disorder reducing red blood cell production.
is a rare inherited bone marrow disorder causing early-onset severe anemia.
is a rare inherited anemia causing low red blood cells from birth.
is a rare inherited bone marrow failure causing early-onset red-cell anemia.
is a rare immune disorder causing enlarged lymph nodes and autoimmunity.
causes hearing loss and low platelets, with symptoms varying by person.
is a rare genetic disorder causing severe spine, rib, and kidney abnormalities.
is a rare condition where the bowel develops thin narrowing bands.
is a rare tumor near the pituitary gland and optic nerves.
is a rare genetic condition causing diaphragm, limb, and skull defects.