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 inherited disorder causing sensorineural hearing loss and ovarian insufficiency.
is a genetic disorder causing parkinsonism, depression, weight loss, and breathing problems.
is a chronic multisymptom illness affecting some veterans after Persian Gulf service.
is a movement disorder causing ongoing muscle contractions and abnormal postures.
is a leftover fetal heart structure that is usually harmless.
is a serious newborn condition causing blood to bypass the lungs.
is a rare birth defect affecting the aorta and blood flow.
is long-lasting swelling of lymph nodes in several areas of the body.
is a rare eye condition where fetal eye tissue remains after birth.
is chronic facial pain without a clear underlying cause.
is a rare heart vein difference that can affect blood flow.
is a rare vein variation that can affect heart blood flow.
is a long-term asthma type with mild but recurring breathing symptoms.
is a long-term lung condition causing ongoing asthma symptoms and flare-ups.
is a rare genetic condition causing uterus and fallopian tubes in males.
is a rare eye condition that can cause lasting central vision loss.
is a rare blood condition with too many noncancerous B cells.
is a long-term asthma type with severe, hard-to-control breathing symptoms.
is a mental health condition affecting thoughts, emotions, behavior, and relationships.
is a highly contagious bacterial infection that causes severe coughing fits.
is a neurodevelopmental condition affecting communication, behavior, and social interaction.
is inflammation of inner knee tendons or bursa (fluid-filled sac) causing pain.
is a rare eye condition causing cloudy corneas and vision problems.
is a rare genetic disorder causing eye problems and developmental differences.