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 affecting brain growth, eye lenses, and development.
is a skin condition causing dry, ring-shaped patches with raised edges.
is a rare skin disorder causing dry, ring-shaped patches with raised edges.
causes scaly spots on the palms, soles, and other skin.
is a rare skin birthmark linked to abnormal sweat gland ducts.
is a group of rare disorders affecting how the body makes heme.
is a liver-related porphyria causing painless sun-triggered blisters and fragile skin.
is a very rare inherited disorder that disrupts heme production.
is a genetic blood pigment (heme) disorder with skin and nerve attacks.
is a rare condition with birthmarks and fluid buildup around the brain.
causes increased pressure in the vein carrying blood to the liver.
is a blood clot in the vein carrying blood to the liver.
is a liver condition affecting small portal blood vessels and pressure.
is a serious whole-body response after cardiac arrest and restored circulation.
is low insulin production after surgery, which can affect blood sugar.
is long-term leg pain, swelling, and skin changes after a deep vein clot.
is a usually Epstein-Barr virus-related lymphoma-like disorder after transplantation.
is hormone deficiency after head injury that can affect growth, energy, fertility.
is a trauma-related condition causing intrusive memories, avoidance, and heightened alertness.
is a rare brain inflammation that can occur after vaccination.
is swelling of lymph nodes behind the ear, usually from infection.
is a rare genetic condition causing facial bone and postaxial limb differences.
is a genetic condition causing an extra, fully formed finger or toe.
is an inherited condition causing an extra small finger or toe.