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 benign uterine tumor beneath the lining, causing heavy bleeding, infertility.
is a heart valve narrowing that reduces blood flow to lungs.
is a noncancerous growth on the uterus’s outer wall.
is a chronic condition involving compulsive use, tolerance, and withdrawal.
is a mental health condition causing hallucinations or delusions after substance use.
is a mental health condition involving harmful use of substances.
is an enlarged thyroid that grows downward behind the breastbone.
is a rare, painful tumor under a fingernail or toenail.
is a narrowing below the aortic valve that blocks blood flow.
is a rare inherited disorder affecting brain signaling, development, and movement.
is a rare inherited disorder causing repeated episodes of dangerous ketoacidosis.
is a rare allergic reaction to the muscle relaxant succinylcholine.
is the sudden, unexplained death of a sleeping infant under one.
is an inherited condition linked to sudden infant death and testicular abnormalities.
is a rapid, unexplained inner ear hearing drop requiring prompt treatment.
is an inherited condition causing unusually short fingers and thumbs.
is an allergic reaction to the antibiotic sulfamethoxazole.
is an allergic reaction to sulfasalazine, sometimes causing rash or breathing trouble.
is an inherited skeletal disorder affecting cartilage, bone growth, and body size.
is a rare blood condition that reduces oxygen delivery and causes cyanosis.
is a rare inherited disorder causing severe brain injury from sulfite buildup.
is a rare genetic disorder causing sulfite buildup and severe neurologic problems.
is a rare inherited disorder causing sulfite buildup and serious brain injury.
is a rare inherited disorder causing severe brain injury in infancy.