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 obesity linked with other medical, developmental, or genetic features.
is a genetic condition causing reduced pigment plus other health problems.
is a rare condition with underdeveloped optic nerves and other body changes.
is a rare genetic condition causing underdeveloped eye sockets and other abnormalities.
is a genetic condition affecting outer eye position and other body systems.
is a rare inherited skin disorder with scaling and other body features.
is a genetic condition affecting the kidneys, urinary tract, and other organs.
is a group of genetic conditions affecting airway or chest development.
is an inherited eye disorder causing vision loss with other body features.
is an inherited condition causing hearing loss and other body problems.
is a wider-than-usual space between the inner eye corners in syndromes.
is a group of birth differences affecting the urinary and reproductive organs.
is an inherited condition affecting development of the uterus and vagina.
is a genetic condition causing internal organ abnormalities with other body changes.
is a genetic eye disorder that can also affect growth and development.
is an inherited condition causing intellectual disability and other health problems.
is a genetic condition causing intellectual disability with other health features.
is a rare inherited condition causing intellectual disability and other developmental differences.
is a rare inherited condition causing intellectual disability and other health problems.
is a rare inherited disorder causing intellectual disability and developmental delay.
is a rare inherited condition affecting learning, development, and sometimes physical features.
is a rare inherited condition affecting learning, development, and physical features.