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 disorder causing albinism and sensorineural hearing loss.
is a genetic disorder causing short stature, shortened bones, sometimes hormone resistance.
is a chronic condition involving uncontrolled drinking, tolerance, and withdrawal symptoms.
is a chronic medical condition affecting control over drinking and health.
involves mental and behavioral changes from alcohol intoxication or withdrawal, often temporary.
are lifelong physical, behavioral, and learning problems from alcohol exposure during pregnancy.
is a brain-based condition from prenatal alcohol exposure, impacting learning and behavior.
is heart muscle enlargement and weakness from long-term heavy alcohol use.
is stomach lining inflammation from alcohol, causing pain, nausea, and indigestion.
is liver inflammation from heavy alcohol use, ranging mild to life-threatening.
is a life-threatening acid-ketone buildup after heavy drinking and poor intake.
is progressive liver scarring from long-term heavy alcohol use.
is nerve damage from long-term alcohol use causing pain, numbness, weakness.
is pancreas inflammation from long-term alcohol use, causing pain and digestive issues.
is a serious alcohol-related brain disorder with hallucinations, delusions, confusion.
is an allergic reaction to an anesthesia muscle relaxant, sometimes severe (anaphylaxis).
is a rare inherited disorder affecting skin, eyes, movement, and development.
is a protein-deposit disease mainly affecting kidneys, causing chronic kidney disease.
is a blood cancer affecting marrow, with few abnormal cells in blood.
is a rare skin infiltration by leukemia cells without blood abnormalities.
is skin involvement by monocytic leukemia without abnormal blood counts.
is a parvovirus infection of mink and ferrets causing immune-mediated illness.
is a rare genetic brain disorder affecting movement, development, and thinking.
is a rare genetic leukodystrophy affecting astrocytes, with early neurological decline.