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.
affects the sense of smell by damaging the nerve for smell.
is a rare cancer that starts high inside the nose.
is a childhood arthritis affecting four or fewer joints, often the knees.
is a male infertility condition with low, poorly moving, abnormally shaped sperm.
is a rare brain tumor with features of two glioma types.
is a rare brain tumor with mixed glioma cell features.
is a rare inherited eye disorder causing poor vision and light sensitivity.
is a usually slow-growing brain tumor arising from supportive nerve cells.
is a rare brain tumor that starts in cells supporting nerves.
is a slow-growing brain tumor with specific genetic changes.
is a rare, slow-growing brain tumor with more aggressive grade 3 features.
is a condition causing six or more missing permanent teeth.
is a genetic condition combining missing teeth (oligodontia) and increased cancer risk.
is a pregnancy complication with too little amniotic fluid around the baby.
is a rare kidney disorder with fewer, enlarged filtering units.
is a group of inherited disorders affecting sugar breakdown in cells.
is a condition with low sperm count that can affect fertility.
is a rare genetic condition affecting the scalp, limbs, and sometimes heart.
is a progressive brain disorder affecting movement, balance, coordination, and speech.
is a rare inherited disorder causing hearing loss and worsening coordination.
is a rare disorder causing multiple benign cartilage tumors in bones.
is a rare inherited immune disorder causing severe infections and skin inflammation.
is a rare genetic bone disorder causing short limbs and short stature.