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 genetic condition affecting hearing, eye color, hair, and skin pigmentation.
is a genetic condition causing hearing loss, pigmentation changes, and wide-set eyes.
is a genetic condition causing hearing loss and changes in eye coloring.
is a genetic condition causing variable congenital hearing loss and pigment differences.
is a genetic condition that can affect hearing and pigment coloring.
is a rare genetic condition causing hearing loss and pigment changes.
is a rare genetic condition causing hearing loss and limb differences.
is a genetic condition with hearing loss, pigment changes, and Hirschsprung disease.
is a rare genetic condition affecting hearing, pigment, and bowel nerves.
is a rare genetic condition affecting pigment, hearing, and bowel nerve cells.
is a rare condition causing hearing loss, pigment changes, and Hirschsprung disease.
is a genetic syndrome causing developmental delays, behavior differences, and facial changes.
is a rare inherited eye disorder causing progressive vision loss.
is a rare genetic condition affecting the eyes, kidneys, and development.
is a rare genetic condition affecting development, learning, and physical features.
is a rare blood cancer that causes too much abnormal antibody.
is cancer in throat lymph tissue around the nose and mouth.
is a rare genetic disorder causing severe muscle, brain, and eye problems.
is a rare inherited disorder affecting brain, eyes, and development.
is a rare inherited genetic disorder causing eye, brain, developmental abnormalities.
is a rare genetic disorder affecting the eyes, brain, and development.
is a rare inherited disorder affecting brain, eye, and reproductive development.
makes blood-thinner treatment less effective, so higher warfarin doses are needed.