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 an inherited blood vessel disorder that can affect the brain.
is an inherited disorder affecting brain blood vessels, causing strokes and dementia.
is a rare disorder causing blood clots and enlarged lung arteries.
is a common viral infection that often causes mild or no symptoms.
is a tick-borne bacterial infection that can cause fever and aches.
is caused by HHV-8 and can lead to certain cancers.
is a viral infection that weakens the immune system over time.
is a viral infection caused by orthopoxviruses, including mpox and cowpox.
is a tick-borne bacterial infection that can cause fever and illness.
is a common viral infection spread through skin-to-skin sexual contact.
is a rare, fatal brain disease caused by abnormal prion proteins.
is a rare birth difference with an absent or underdeveloped upper arm.
is a rare birth condition where the upper and forearm bones fuse.
is a rare birth condition where arm bones are fused together.
is a rare birth condition where elbow bones are joined together.
is a rare condition where both elbow joints are fused before birth.
is a rare birth difference where one elbow's arm bones are fused.
is a rare birth difference where part of the elbow is missing.
is a very rare genetic syndrome that can affect growth and development.
is a condition associated with HTT and SLC2A3. This condition is also known as Huntington chorea.
is a rare inherited brain disorder causing movement, thinking, and behavior changes.
is a rare inherited brain disorder causing movement, thinking, and mood problems.
is a rare inherited brain disorder causing movement, thinking, and behavior problems.
is an inherited disorder causing progressive movement, thinking, and mood problems.