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 lymphoma affecting the brain, eyes, spinal cord, or meninges.
is a chronic eye disease slowly damaging the optic nerve, impairing sight.
is an inherited eye disorder that damages the optic nerve and vision.
is a rare cancer that starts in one organ or tissue.
causes symptoms when standing upright, often improving with sitting or lying down.
is a blood pressure disorder causing dizziness or fainting when standing.
is a rare condition causing fast leg tremors only when standing.
is a rare disorder that causes progressive bone loss and related problems.
is reduced ovarian function before 40, causing infertility and menopause-like symptoms.
is a condition where the ovaries stop working normally too early.
causes ovaries to stop working normally before age 40.
is an inherited condition causing reduced ovarian function and often infertility.
is a genetic condition causing early loss of normal ovarian function.
causes the ovaries to stop working normally before age 40.
is when the ovaries stop working normally before age 40.
causes the ovaries to stop working properly before age 40.
is a genetic condition causing early ovarian function loss and infertility.