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 genetic condition causing kidney failure and Wilms tumor risk.
is a mental health condition involving strong needs for reassurance and support.
causes persistent feelings of being detached from yourself or your surroundings.
is a mood disorder causing persistent sadness and loss of interest.
is vision loss from blocked visual input during early childhood.
is a rare skin blood vessel malformation causing soft, dark, raised spots.
is skin inflammation causing itchy, red, sometimes swollen or scaly rash.
is an intensely itchy, blistering skin rash linked to gluten sensitivity.
is a rare, slow-growing skin cancer that starts in connective tissue.
is a common skin condition causing raised, itchy welts after scratching.
is a rare inherited disorder affecting the skin and brain white matter.
is a fungal infection of the skin, hair, or nails.
is an autoimmune disease causing muscle weakness and a distinctive skin rash.
is a rare inherited disorder causing loose skin and bone loss.
is a rare inherited disorder affecting skin, hair, and nails.
is a common fungal infection affecting the skin, hair, or nails.
is a harmless skin condition causing dark bumps, usually on the face.
is a rare genetic disorder causing very fragile, sagging skin and bruising.
affects the skin's deeper layer, causing changes that vary by cause.
is a skin connective tissue disorder causing loose, stretchy, fragile skin.
is a growth in the skin's deeper layer that may be benign.
is a rare inherited condition affecting the cornea, cartilage, and skin.
is a usually harmless growth containing skin-like tissue, often present at birth.
is a usually benign ovarian growth containing skin, hair, or fat.