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.
causes flu-like and thinking symptoms after orgasm or ejaculation.
is a mood disorder causing sadness, anxiety, and bonding difficulties after childbirth.
is a rare, severe mental health emergency that can occur after childbirth.
is a late complication causing new muscle weakness, fatigue, and pain.
is low thyroid hormone levels after surgery affecting part or all thyroid.
are inherited disorders that impair nerve-muscle signaling, causing muscle weakness and fatigue.
is brain inflammation after transplant causing seizures, confusion, and memory problems.
is a flexible rounding of the upper back caused by poor posture.
causes a rapid heartbeat and dizziness when standing up.
is an itchy skin reaction caused by allergy to potassium dichromate.
causes muscle stiffness (myotonia) worsened by potassium, from SCN4A gene changes.
is a rare genetic disorder affecting bone, brain, and development.
results from low amniotic fluid, often affecting kidney and lung development.
is inflammation of an internal pouch, often causing diarrhea and belly pain.
is a rare tick-borne brain infection that can cause severe illness.
is a rare tumor that can make too many stress hormones.
is a genetic condition caused by missing expression of paternal genes.
is a rare genetic disorder caused by two maternal chromosome 15 copies.
is a genetic disorder caused by missing paternal genes on chromosome 15.
is a genetic condition causing low muscle tone, overeating, and developmental challenges.
is a genetic condition causing low muscle tone, overeating, and learning difficulties.
is a rare genetic disorder causing low muscle tone, overeating, and delays.
is a rare genetic condition causing obesity, developmental delays, and behavior differences.
is a rare inherited eye condition with tiny corneal deposits, often harmless.