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 usually harmless skin cyst containing tissue like hair or oil.
is a rare, usually benign cyst in the brain or spinal cord.
is a rare genetic condition affecting skin, teeth, and hair development.
is a rare genetic condition affecting hair, skin, and sometimes nails.
is a rare inherited skeletal disorder causing short stature and joint laxity.
is cancer in the lower part of the large intestine.
is a rare inherited muscle disease that can also affect the heart.
is a genetic muscle disease (myopathy) causing weakness, heart, and breathing problems.
is a rare tumor that grows in connective tissue and can recur.
is a rare, usually slow-growing brain tumor that affects infants.
is a rare, usually noncancerous brain tumor affecting infants and young children.
is a rare, aggressive cancer that usually starts in the abdomen.
is a type of childhood brain tumor that starts in the cerebellum.
is a very rare genetic disorder affecting cholesterol production and development.
is a rare smoking-related lung disease that causes inflammation and breathing problems.
is a bladder control problem where bladder and sphincter muscles miscoordinate.
is a group of severe brain disorders causing seizures and developmental delays.
is a rare genetic brain disorder causing seizures and developmental delays.
is a rare genetic condition causing seizures and developmental problems.
is a genetic brain disorder causing developmental delays and seizures.
is a genetic brain disorder causing seizures and developmental problems.
is a rare genetic brain disorder causing seizures and developmental delay.