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 difference in sex development affecting genes, hormones, and reproductive anatomy.
is a genetic condition in males with an extra Y chromosome.
is a rare sex chromosome condition causing developmental delays and low testosterone.
is a rare sex chromosome condition causing developmental, learning, and hormonal differences.
is a rare sex chromosome condition with variable developmental and learning challenges.
is a rare sex chromosome condition in males with developmental delays.
is a rare sex chromosome condition causing developmental, learning, and health challenges.
is a rare chromosomal condition in males causing developmental and physical differences.
is a rare genetic disorder causing myelin loss (hypomyelination), dental, hormonal problems.
is a rare chromosome 4 microduplication causing variable developmental and physical differences.
is a rare chromosomal disorder causing developmental delay and growth problems.
is a rare chromosome 4 deletion causing developmental and congenital differences.
results from 5-FU overdose or sensitivity, with potentially life-threatening toxicity.
is a rare inherited metabolic disorder disrupting the glutathione (antioxidant) cycle.
is a rare genetic condition causing developmental delays and variable health issues.
is a rare genetic disorder from missing 5q14.3 DNA, causing developmental delays.
is a rare chromosomal duplication causing developmental delays and variable congenital features.
is a rare enzyme disorder causing episodic hemolytic anemia under oxidative stress.
is a rare inherited metabolic disorder disrupting phenylalanine and neurotransmitters.
is a rare chromosome 6 deletion causing developmental, speech, and learning delays.
is a rare chromosome 6 deletion causing developmental delays and birth differences.
is a genetic condition from missing chromosome 6 material causing developmental challenges.
is a rare genetic condition causing developmental delays and variable congenital features.
is a rare chromosome change causing developmental delays, speech challenges, variable features.