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 seizures and developmental difficulties.
is a rare genetic disorder causing seizures and delayed development.
is a rare genetic disorder causing seizures and developmental problems.
is a rare genetic disorder causing seizures and developmental challenges.
is a rare genetic brain disorder causing seizures and developmental delays.
is a rare genetic condition causing seizures and developmental problems.
is a rare genetic condition causing seizures and developmental delays.
is a genetic brain disorder causing developmental delays and hard-to-control seizures.
is a genetic brain disorder causing seizures and developmental problems.
is a rare genetic disorder causing seizures and developmental delays.
is a rare genetic brain disorder causing seizures and developmental problems.
is a rare genetic condition causing seizures and developmental difficulties.
is a genetic brain disorder causing seizures and developmental delays.
is a rare brain condition causing seizures and developmental problems.
