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 benign conjunctival growth onto the cornea, linked to UV exposure.
is a rare eye surface cancer that can affect vision.
affects eye surface blood vessels, causing redness, irritation, swelling, or bleeding.
is inflammation of the conjunctiva (pink eye), causing redness and discharge.
is age-related loosened conjunctiva causing eye irritation, tearing, and discomfort.
causes excess aldosterone, leading to high blood pressure and low potassium.
is a noncancerous growth from connective tissues, usually slow-growing and localized.
is a rare cancer starting in connective tissues like muscle, fat, bone.
is a group of autoimmune and genetic disorders affecting connective tissues.
is a rare collagen disorder from lysyl hydroxylase-3 (PLOD3) deficiency.
is a rare genetic bone disorder causing short stature and spinal abnormalities.
are congenital heart defects affecting the heart’s outflow tracts and arteries.
is persistent eye bulging (proptosis), often from thyroid eye disease.
is a lifelong anemia caused by inherited problems with iron handling.
is a rare inherited anemia causing lifelong low red blood cells.
is a rare inherited disorder causing abnormal red cell production and anemia.
is an inherited blood disorder causing fragile spiky red cells and anemia.
is an inherited folate-processing disorder causing megaloblastic anemia and developmental problems.
is a rare inherited disorder of vitamin B12 processing causing megaloblastic anemia.
is a rare inherited disorder causing megaloblastic anemia and severe neurologic disease.
is a rare inherited disorder from DNA repair defects, causing childhood cancers.
is a benign, lifelong low white blood cell (neutrophil) count.
is a genetic disorder causing chronic low neutrophils (neutropenia) and systemic features.
is a genetic blood disorder causing anemia due to impaired iron use.