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 4.
causes extra genetic material on chromosome 5, leading to varied health problems.
is a rare genetic condition caused by extra material on chromosome 6q.
is a rare genetic condition caused by extra material on chromosome 7q.
is a rare genetic condition caused by extra material on chromosome 8.
is a rare chromosome condition that can affect development, growth, and health.
is a rare chromosome condition causing developmental and health differences.
is a rare genetic condition caused by extra material on chromosome 1p.
is a rare genetic condition caused by extra material on chromosome 10p.
is a rare chromosomal condition causing developmental and health differences.
is a rare chromosome change that can affect growth, development, and health.
is a rare genetic condition caused by extra material on chromosome 17.
is a rare genetic condition caused by extra material on chromosome 19p.
is a rare genetic condition caused by extra material on chromosome 2.
is a rare chromosome change causing developmental and health problems.
is a rare chromosome change causing variable developmental and health problems.
is a rare genetic condition caused by extra material on chromosome 6.
is a rare genetic condition caused by extra material on chromosome 7p.
is a rare chromosomal condition caused by extra genetic material on Xp.
involves extra chromosome 18 material that can affect development and health.
is a rare chromosome change causing varied developmental and health problems.
is a rare genetic condition caused by extra material from chromosome 9.
is a rare chromosome change that can affect development and health.