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.
causes congenital hearing loss, balance problems, and progressive vision loss.
is an inherited condition causing hearing loss and progressive vision problems.
is inherited, with moderate hearing loss and progressive vision loss.
is inherited, with moderate hearing loss, progressive vision loss, and normal balance.
is an inherited condition causing hearing loss and progressive vision loss.
causes progressive hearing and vision loss, sometimes with balance problems.
is a rare inherited condition causing progressive hearing, vision, and balance problems.
is an inherited disorder with progressive hearing, vision loss, and balance problems.
is a rare genetic immune disorder causing severe inflammation early in life.
is a rare cancer affecting the ovaries, fallopian tubes, or nearby tissues.
is a noncancerous growth in the uterus that may cause symptoms.
is a rare cancer of the uterus with mixed tumor types.
is cancer that starts in the tissues of the uterus.
is a rare, aggressive cancer of the uterus needing prompt specialist care.
is a rare birth condition where the cervix is missing or underdeveloped.
is white patches on the cervix that need medical evaluation.
is a rare tumor of the uterus with glandular and fibrous tissue.
is a rare, usually noncancerous tumor of the uterus.
is a rare, benign tumor that forms in the uterus.
is a rare cancer of the uterus with glandular and sarcoma tissue.
is a benign uterine fibroid with sudden bleeding and tissue damage.
is a rare, usually noncancerous uterine growth with abnormal glands and muscle.
is a rare, usually noncancerous uterine smooth muscle tumor with unusual cells.
is cancer that starts in the lining or body of the uterus.