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 group of diseases that damage nerves controlling movement.
is nerve damage causing muscle weakness, cramps, and movement problems.
are repeated, often rhythmic movements that usually begin in early childhood.
is a rare lung condition causing enlarged airways and repeated infections.
is an infection or condition affecting the mouth, causing pain or sores.
is a movement disorder that affects how a person moves.
is a rare genetic condition causing developmental delay and multiple congenital anomalies.
is a rare genetic condition affecting development, learning, and body systems.
is a rare blood vessel disorder that reduces brain blood flow.
is a rare genetic syndrome affecting brain vessels, growth, and sexual development.
is a rare brain vessel disorder causing reduced blood flow and strokes.
is a rare disorder causing narrowed brain arteries and swallowing problems.
is a very rare genetic syndrome that causes multiple birth differences.
is a rare inherited disorder affecting sugar processing and many body systems.
is a rare inherited disorder affecting sugar processing, especially in the liver.
is a contagious viral infection that usually causes rash and flu-like symptoms.
is a rare inherited eye disorder that can cause progressive vision loss.
is an inherited condition causing colon polyps and higher colorectal cancer risk.
is a rare inherited mitochondrial disorder causing leg stiffness, weakness, and neuropathy.
is a genetic condition causing developmental delay, seizures, microcephaly, and short stature.
is a rare immune system cancer involving abnormal antibodies.
is a rare B-cell disorder that makes abnormal antibody heavy chains.
is an inherited kidney disease that slowly worsens kidney function over time.