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 condition causing blocked sperm flow and infertility.
is a rare genetic disorder that can cause crossed eyes (strabismus).
is a rare inherited movement disorder causing involuntary muscle contractions and twisting.
is an inherited hormone disorder that can affect growth and metabolism.
is a group of inherited seizure disorders that often begin early.
is a rare inherited eye disease that can affect vision.
is a rare inherited condition that causes abnormal eyelid positioning.
is a rare genetic condition that can affect female fertility.
is a rare inherited digestive disorder that affects the stomach or intestines.
are uncommon inherited conditions affecting female reproductive health, fertility, pregnancy, or childbirth.
is a rare inherited condition that can cause severe headaches.
is a rare inherited blood disorder that affects blood cells.
is a rare inherited liver disease.
is a rare inherited condition causing involuntary movements and related neurologic symptoms.
is a rare inherited disorder affecting hormone control in the brain.
is a rare inherited immune disorder that weakens the body's defenses.
is a rare inherited eye condition causing corneal inflammation and vision problems.
is a rare genetic condition that affects learning, development, and daily life.
is a rare inherited eye condition affecting the macula, central vision.
is a rare genetic condition that can cause male infertility.
is a rare inherited disorder affecting the spinal cord or bone marrow.
is a rare genetic disorder causing abnormal movements and sometimes developmental problems.
is a rare inherited disorder causing sudden muscle jerks and movement problems.
is a rare genetic neurological disorder affecting the brain and nerves.