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 immune weakness, chromosomal instability, facial differences.
is an inherited disorder causing immune problems, developmental delays, and facial differences.
is a rare inherited disorder affecting immunity, chromosomes, and facial development.
is a small-vessel inflammation causing rash, joint pain, abdominal pain, kidney problems.
is a rare immune disorder causing low antibodies and frequent infections.
is a rare disorder where abnormal antibodies build up in organs.
is a disorder where abnormal proteins build up and damage organs.
is a kidney disease caused by immune deposits that damage filters.
is a rare kidney disease caused by abnormal protein deposits.
is a rare kidney disease caused by protein deposits in the filters.
is inflammation of the pituitary gland caused by some cancer immunotherapy drugs.
is a birth defect where the anal opening is missing or blocked.
is a rare birth disorder affecting the mouth, ribs, and spine.
is a common, highly contagious skin infection causing sores and crusting.
is a rare, serious pregnancy-related rash with pus-filled bumps.
is erectile dysfunction (ED), causing persistent trouble getting or keeping erections.
are genetic conditions caused by problems with parent-specific gene activity.
is an early-stage cancer that has not spread beyond its origin.
is a hormone disorder causing water retention and low blood sodium.
is a rare infant heart rhythm disorder causing a persistently fast heartbeat.
is a rare disease with progressive muscle weakness and brain white-matter abnormalities.
is an inherited disorder affecting muscles, bones, and sometimes brain function.
is a rare inherited disorder affecting muscles, bones, and sometimes thinking.