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 inflammation of the spine and joints, causing pain and stiffness.
is an inflammatory autoimmune condition affecting the tear-producing glands.
is a contagious viral infection affecting the nose, throat, and lungs.
is a cancer in the lower back part of the brain.
is an inflammation of the pituitary causing hormone imbalance and excessive thirst.
is a rare basal cell skin cancer with small, deep cyst-like tumors.
is a groin hernia where intestine or fat protrudes through muscle.
is a serious infection caused by breathing in anthrax spores.
is a rare but serious infection caused by breathing in anthrax spores.
is a rare, serious illness caused by inhaling botulinum toxin.
is an inherited blood cancer that starts in the bone marrow.
is a genetic condition that increases the risk of certain cancers.
is an inherited syndrome that greatly raises cancer risk from BRCA2 changes.
is a genetic prion disease causing rapid dementia, movement problems, and death.
is an inherited condition that raises the risk of digestive cancers.
is an inherited skin condition causing fragile skin and painful blistering.
is an inherited condition that raises the risk of certain gynecologic cancers.
is a genetic condition that raises the risk of blood cancers.
is a rare inherited brain disease caused by abnormal prion proteins.
is an inherited skin disorder causing dry, scaly, thickened skin.
is an inherited disorder causing scaly skin and other health problems.
is a rare inherited condition causing reduced adrenal hormone production.
is a genetic condition that affects how the body processes nutrients.
is an inherited condition that raises the risk of nervous system tumors.