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 group of inherited disorders that affect bone growth and strength.
is a rare inherited brainstem or cerebellar disorder often affecting the eyes.
is a rare inherited blood vessel condition causing capillary birthmarks.
is an inherited heart condition that can affect rhythm and function.
is a rare genetic condition that can cause high blood pressure.
is a rare inherited eye condition affecting the choroid and vision.
is an inherited bleeding disorder that affects how blood clots.
is a rare inherited eye disorder affecting the cornea and vision.
is a rare inherited hearing loss caused by gene changes.
is a rare genetic developmental problem that begins during embryonic development.
is a group of inherited forms of diabetes caused by gene changes.
is a genetic condition that can affect the body in different ways.
is a rare inherited disorder that often causes sudden muscle jerks.
is a rare genetic disorder affecting multiple parts of the eye.
is a rare genetic disorder affecting the front part of the eye.
is a rare genetic disorder affecting the tear-drainage system.
is a rare genetic disorder affecting tissues around the eyes.
is a rare inherited eye condition affecting the back of the eye.
is a rare genetic eye disorder affecting the pupil's normal shape.
is a rare inherited condition that affects eye development and vision.
is a rare genetic condition that mainly affects the eye's conjunctiva.
is a rare genetic disorder that mainly affects the cornea.
is a rare genetic disorder that can cause inward-turning eyelids.
is a rare genetic disorder that causes clouding of the eye lens.