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 nerve problem that affects feeling and movement in the hand.
is a rare, harmless lump in the center of the upper lip.
is a harmless smooth red patch in the middle of the tongue.
is a cancer that starts in the area between the lungs.
is a rare, usually benign tumor that develops in the chest.
is a rare cancer with features between Hodgkin and non-Hodgkin lymphoma.
is excess fat buildup in the chest around central organs.
is a cancer of lymph tissue in the chest between the lungs.
is a rare, usually benign pigmented nerve sheath tumor in the chest.
is a rare tumor of connective tissue in the chest cavity.
is a usually benign nerve sheath tumor that grows in the chest.
is a rare cancer that forms bone-like tissue in the chest.
is a rare, usually benign nerve sheath tumor in the chest.
is a serious infection or inflammation in the area between the lungs.
is a rare cancer of blood vessel cells in the chest.
is a rare nerve tissue tumor in the chest (mediastinum).
is a rare, usually noncancerous smooth muscle tumor in the chest.
is a rare cancer of smooth muscle tissue in the chest.
is a rare cancer of fatty tissue in the chest cavity.
is a rare childhood cancer arising from nerve cells in the chest.
is a usually benign nerve sheath tumor in the chest area.
is a rare cancer of muscle-like tissue in the chest.
is a rare cancer that starts in tissues in the chest cavity.
is a rare germ cell tumor that develops in the chest.