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 an inherited condition causing fragile skin, woolly hair, and thick palms.
is a rare, usually benign skin growth from blood vessel cells.
is a rare, usually benign skin tumor that can cause severe pain.
is a usually benign skin growth from nerve-related cells.
is a benign growth of extra blood vessels in the skin.
is a harmless lump of fatty tissue under the skin.
is a serious skin cancer from melanocytes, often linked to UV.
is a rare growth of meningioma tissue in or under skin.
is a rare skin cancer showing features of basal and oil glands.
is a usually harmless skin growth caused by overgrowth of surface cells.
is a rare skin cancer arising from hair follicle cells.
is an inflammatory condition causing raised skin bumps, patches, or nodules.
is a rare cancer that starts in the skin’s connective tissues.
is a common skin cancer that can usually be treated successfully.
are harmless, soft skin growths that commonly appear in skin folds.
affects blood vessels in the skin, causing color changes, spots, or swelling.
is a rare cancer that starts in the bones beneath the brain.
is a rare, slow-growing bone cancer at the base of the skull.
is a usually slow-growing tumor in the tissues at the skull base.
is a rare cancer that starts in the skull bones or tissues.
is a lung disease caused by long-term inhalation of slate dust.
is a genetic condition causing developmental delay, intellectual disability, and hearing loss.
is an inherited condition causing developmental delay, feeding problems, and hearing loss.
is a rare genetic condition causing developmental delays, intellectual disability, and deafness.