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 condition caused by extra material on chromosome 17.
is a rare chromosome condition caused by extra material on chromosome 19.
is a rare genetic condition caused by extra chromosome 2 material.
is a rare genetic condition caused by extra chromosome 20 material.
is a rare genetic condition caused by extra chromosome 3 material.
is a genetic condition caused by extra chromosome 4 material.
is a rare genetic condition caused by extra chromosome 6 material.
is a rare genetic condition caused by extra chromosome 7 material.
is a rare genetic condition caused by extra chromosome 8 material.
is a rare genetic condition caused by extra X chromosome material.
is a rare genetic condition caused by extra material on chromosome 1q.
is a rare genetic condition caused by extra material on chromosome 10q.
is a rare genetic condition caused by extra chromosome 11q material.
is a rare genetic condition caused by extra material on chromosome 13.
is a rare chromosome change causing developmental and health problems.
is a rare chromosome condition caused by extra material on chromosome 15.
is a rare chromosome condition causing varied developmental, growth, and health problems.
is a rare genetic condition caused by extra material on chromosome 17q.
is a rare genetic condition caused by extra material on chromosome 18q.
is a rare genetic condition caused by extra material on chromosome 19q.
is a rare genetic condition caused by extra material on chromosome 2.
is a rare genetic condition caused by extra material on chromosome 20.
is a rare genetic condition caused by extra material on chromosome 22.
is a rare genetic condition caused by extra material on chromosome 3.