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 birth defect affecting how the eye develops before birth.
is a genetic condition causing developmental delays, seizures, and sometimes movement problems.
is a rare inherited condition causing developmental delay and other symptoms.
is a genetic condition causing developmental delays, autism features, and unsteady walking.
is a genetic condition causing developmental delay and distinctive facial features.
is a rare inherited disorder causing developmental delay, immune problems, and leukoencephalopathy.
causes delayed development, low muscle tone, and trouble with speech.
causes delayed development, poor growth, and distinctive facial and body features.
is a broad term for conditions affecting mental, emotional, and social development.
is a rare genetic disorder causing birth defects, hearing loss, and dystonia.
is a rare condition where the heart points toward the right side.
is a rare condition causing extreme thirst and large amounts of urine.
is a chronic condition causing high blood sugar from insulin problems.
damages blood vessels from diabetes, increasing risks to eyes, kidneys, and heart.
is a cataract linked to diabetes that can blur vision.
is birth differences in a baby caused by diabetes during pregnancy.
is a diabetes-related brain complication that can affect memory, mood, and thinking.
is a serious diabetes complication causing dangerous acid buildup from insulin shortage.
is an eye complication of diabetes that can blur central vision.
is nerve damage caused by diabetes, often affecting the feet and legs.
is diabetes-related eye disease damaging retina's blood vessels, risking vision loss.
is a rare genetic bone marrow disorder causing early-onset red-cell anemia.
is a rare inherited bone marrow failure causing early severe anemia.
is a rare genetic disorder causing severe macrocytic anemia in infancy.