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 syndrome often causing high blood pressure in the lungs.
is a rare genetic condition causing fused bones or abnormal joints.
is a rare genetic condition affecting hair, skin, and sometimes the heart.
is an inherited immune disorder causing very low antibodies and other problems.
is a rare genetic condition causing underdeveloped irises and other health problems.
is a rare birth condition causing fused eyelids and other abnormalities.
is a group of birth defects affecting the anus and other organs.
is a rare immune disorder causing severe diarrhea and other autoimmune problems.
is a rare condition causing blocked bile ducts and other birth differences.
is a genetic condition with underdeveloped or absent breasts and other features.
is cataracts occurring with other health problems as part of a syndrome.
is an inherited eye disorder causing vision loss with other body features.
is a rare inherited disorder causing severe diarrhea and other health problems.
is an inherited condition causing lifelong low platelets and other health problems.
is an inherited eye disorder causing corneal clouding with other body features.
is a genetic condition causing early skull fusion and other body differences.
is a group of birth defects affecting the diaphragm or abdominal wall.
is a group of birth conditions affecting the diaphragm or chest.
is a rare genetic condition causing chronic diarrhea and other body-wide problems.
is a genetic condition that causes crossed eyes and other health issues.
is a condition causing a displaced eye lens with other body features.
is a genetic condition with inner eye folds and other health features.
is a group of birth defects affecting the esophagus and other organs.
is a rare genetic condition causing a gap in the eyelid.