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.
are cortical malformations causing seizures, developmental delays, and vision problems.
is a blockage of the gallbladder that can cause pain and infection.
is a blockage in neck arteries supplying the brain, raising stroke risk.
is a rare inherited eye disease causing progressive central vision loss.
is a work-related lung inflammation caused by breathing in allergens.
is asthma caused or triggered by breathing in workplace dust, fumes, or chemicals.
is a skin condition caused by workplace irritants or allergies.
is a rare genetic disorder causing urinary problems and an upside-down smile.
is a condition causing dark pigment buildup in connective tissues.
is an inherited eye condition causing low pigmentation and vision problems.
is an inherited eye condition causing reduced vision and light sensitivity.
is a rare inherited condition affecting eye pigment and later hearing.
is a rare inherited condition causing vision problems and hearing loss.
is a rare genetic disorder affecting the eyes, nerves, and development.
is cancer that starts in the eye and can affect vision.
is a rare autoimmune disease causing scarring of the eye surface.
is a genetic disorder causing corneal cystine crystals and light sensitivity (photophobia).
causes redness of the eye from increased blood flow.
is higher-than-normal pressure inside the eye without glaucoma damage.
is lower-than-normal eye pressure that may or may not cause problems.
is a rare eye cancer that starts in pigment-making cells.
is a rare eye movement disorder causing trouble quickly shifting gaze.
is a rare eye infection caused by tuberculosis bacteria.
is a rare birth condition affecting facial, ear, eye, and spine development.