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 chromosome condition that can affect development and health.
is a rare chromosome disorder affecting development, learning, and physical features.
is a rare chromosome condition causing developmental delay and birth differences.
is a rare genetic condition caused by extra material on chromosome 11q.
is a rare chromosome condition that can affect growth, development, and health.
is a rare genetic condition caused by extra material on chromosome 14.
is a rare chromosome change that can affect development and health.
is a rare chromosome condition causing developmental delays and variable birth defects.
is a rare chromosome condition causing developmental delays and birth differences.
is a rare genetic condition caused by extra material on chromosome 18.
is a rare chromosome condition causing developmental and health differences.
is a rare genetic condition caused by extra material on chromosome 22.
is a rare genetic condition caused by extra material on chromosome 2.
is a rare genetic condition caused by extra chromosome 3 material.
is a rare genetic condition caused by extra material on chromosome 4.
is a rare genetic condition caused by extra material on chromosome 5.
is a rare chromosome condition caused by extra genetic material on 6p.
is a rare chromosome condition causing developmental delays and other health problems.
is a rare chromosome condition causing developmental delays and varied birth differences.
is a rare chromosome condition causing developmental, learning, and physical differences.
is a rare chromosomal condition that can affect development and health.