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 inherited disorder affecting glutathione production and causing metabolic problems.
is a rare inherited disorder that affects glutathione production and cell protection.
is a term for reactions after eating gluten-containing foods.
is a rare genetic disorder affecting how the body breaks down glycerol.
is a rare inherited disorder affecting glycerol breakdown, often with mild symptoms.
is an inherited disorder that affects glycerol breakdown and energy balance.
is a genetic disorder causing high glycine, seizures, and developmental disability.
is an inherited condition that affects how the body stores sugar.
is a rare inherited disorder that affects how the body stores sugar.
is a rare inherited disorder causing glycogen buildup, especially in muscles.
is a rare inherited disorder causing severe muscle weakness and heart problems.
is an inherited disorder causing progressive muscle weakness and breathing problems.
is a rare inherited disorder affecting muscle energy and red blood cells.
is a genetic disorder causing severe low blood sugar and liver enlargement.
is an inherited metabolic disorder causing fasting hypoglycemia and enlarged liver.
is an inherited disorder causing low blood sugar, enlarged liver, and infections.
is an inherited disorder that disrupts glycogen storage in liver and muscles.
is a rare inherited disorder causing progressive muscle weakness and nerve problems.
is an inherited disorder causing liver disease, muscle weakness, and abnormal glycogen.
is an inherited disorder causing muscle weakness from glycogen buildup in childhood.
is a rare inherited disorder causing severe muscle weakness from birth.
is a rare inherited disorder causing severe muscle weakness before birth.
is a rare inherited liver glycogen disorder that usually does not worsen.
is an inherited disorder causing harmful glycogen buildup and worsening liver disease.