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 missing part of chromosome 8.
is a rare chromosomal condition causing developmental and health problems.
is a chromosomal condition caused by missing part of the X chromosome.
is a rare genetic condition caused by missing material on chromosome 1.
is a rare genetic condition caused by missing material on chromosome 10.
is a rare genetic condition caused by missing material on chromosome 11.
is a rare genetic condition caused by missing material on chromosome 12q.
is a rare genetic condition caused by missing chromosome 13 material.
is a rare genetic condition caused by missing material on chromosome 14.
is a rare genetic condition caused by missing material on chromosome 15.
is a rare genetic condition caused by missing material on chromosome 16q.
is a rare genetic condition caused by missing material on chromosome 17q.
is a rare genetic condition caused by missing material on chromosome 18.
is a rare genetic condition caused by missing material on chromosome 19q.
is a rare genetic condition caused by missing chromosome 2 material.
is a rare chromosome disorder caused by missing material on chromosome 20.
is a rare genetic condition caused by missing material on chromosome 21.
is a rare genetic condition caused by missing chromosome 22 material.
is a rare genetic condition caused by missing material on chromosome 3.
is a rare genetic condition caused by missing material on chromosome 4q.
is a rare genetic condition caused by missing chromosome 5q material.
is a rare genetic condition caused by missing chromosome 6 material.
is a rare genetic condition caused by missing material on chromosome 7q.
is a rare genetic condition caused by missing material on chromosome 8.