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.
causes low thyroid hormone from pituitary gland development or function problems.
is an inherited thyroid disorder causing low hormone levels and slow metabolism.
is a rare metabolic disease causing weak muscles, lactic acidosis, hyperammonemia.
is a rare genetic disorder causing low muscle tone and cystine stones.
is a rare inherited disorder causing low muscle tone and cystinuria.
is a rare genetic condition causing low muscle tone, poor growth, microcephaly.
is a genetic disorder causing low muscle tone and severe developmental delay.
is a rare genetic condition causing low muscle tone, ataxia, and delays.
is an inherited condition causing very sparse scalp and body hair.
is a rare genetic condition causing unusually sparse scalp and body hair.
is a rare inherited condition causing sparse scalp and body hair.
is a genetic condition causing sparse scalp hair and reduced body hair.
is a rare genetic condition causing very sparse scalp and body hair.
is a rare genetic condition causing sparse scalp and body hair.
is a rare genetic condition causing sparse hair growth from childhood.
is a genetic condition causing sparse scalp hair, eyebrows, and eyelashes.
is a rare inherited condition causing sparse scalp hair from childhood.
is reduced or missing eyelash growth on one or both eyelids.
is a rare genetic condition causing progressive scalp hair loss.