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 material on chromosome 9.
is a genetic condition caused by missing part of chromosome X.
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 12.
is a rare genetic condition caused by missing chromosome 16p material.
is a rare chromosomal disorder caused by missing DNA on chromosome 17.
is a rare genetic condition caused by missing chromosome 18 material.
is a rare genetic condition caused by missing chromosome 19p material.
is a rare genetic condition caused by missing material on chromosome 2p.
is a rare genetic condition caused by missing material on chromosome 20.
is a rare chromosomal condition causing developmental delays and birth differences.
is a rare genetic disorder caused by missing chromosome 4 material.
results from missing genetic material on chromosome 5 and affects development.
is a rare genetic condition caused by missing material on chromosome 6.
is a rare genetic condition caused by missing material on chromosome 7.
is a rare genetic condition caused by missing material on chromosome 8.
is a rare condition caused by missing part of the X chromosome.
is a rare genetic condition causing varied developmental, growth, and health problems.
is a rare genetic condition caused by extra material on chromosome 10.
is a rare genetic condition caused by extra material on chromosome 11.
is a chromosome disorder causing extra genetic material and varied symptoms.