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 condition causing learning and developmental challenges, mainly in males.
is an inherited condition causing intellectual disability without other major features.
is an inherited condition causing learning problems and intellectual disability.
is an inherited condition causing learning difficulties without other major features.
is an inherited X-linked condition causing intellectual disability without other major features.
is an inherited condition causing intellectual disability, mainly in males.
is an inherited condition causing intellectual disability without other major physical features.
is a rare inherited condition linked to learning and developmental difficulties.
is an inherited condition causing learning difficulties without other major physical features.
is a rare inherited condition causing intellectual disability without other major features.
is a rare inherited condition causing intellectual disability, mainly in males.
is a genetic condition causing intellectual disability without other major features.
is a rare inherited condition causing learning difficulties and developmental delay.
is an inherited condition causing learning and developmental difficulties, mainly in males.
is a rare inherited condition affecting learning and development, usually in males.
is a rare inherited condition causing learning and developmental difficulties.
