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 condition causing intellectual disability and developmental delays.
is a rare inherited condition causing intellectual disability and developmental delay.
is a rare inherited condition causing intellectual disability, mainly in males.
is a rare inherited condition causing intellectual disability and sometimes delayed development.
is a rare inherited condition causing intellectual disability, usually in males.
is a rare inherited condition causing developmental delay and learning problems.
is a rare inherited condition causing intellectual disability, often in males.
is an inherited condition causing intellectual disability, mainly affecting boys and men.
is an inherited condition causing intellectual disability and speech or behavior differences.
is a rare inherited condition causing intellectual disability, mainly in boys.
is an inherited disorder causing keloid scars, stiff joints, and eye changes.
is a rare inherited skin disorder causing bumps and scarring hair loss.
is a rare inherited disorder causing severe fetal webbing, contractures, and death.
is a rare genetic brain disorder causing severe developmental problems.
is a rare genetic disorder affecting brain development and genital formation.
is a rare inherited immune disorder causing severe reactions to certain infections.
is a rare inherited immune disorder causing severe reactions to some infections.