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 genetic condition affecting the eyes, palate, and brain.
is a rare genetic condition affecting eye development and hearing.
is a rare genetic condition affecting facial, eye, and ear development.
is a rare condition affecting facial, ear, spine, and arm development.
is a rare genetic disorder affecting skin, eyes, and brain development.
is a rare genetic disorder causing reduced pigmentation and brain-related problems.
is a rare congenital disorder affecting the eyes, brain, and skin.
is a rare genetic disorder causing eye, brain, facial differences, developmental delays.
is a rare genetic disorder affecting eyes, brain, and kidneys.
is an inherited condition causing reduced pigment in skin, hair, and eyes.
is an inherited disorder causing low melanin, light coloring, and vision issues.
is a genetic condition causing absent melanin, very light coloring, vision problems.
is an inherited condition causing reduced melanin in skin, hair, and eyes.
is an inherited condition affecting skin, hair, and eye coloring.
is a rare inherited condition causing less pigment in skin, hair, eyes.
causes reduced pigment in the eyes, skin, and hair from birth.
is a rare inherited condition affecting skin, hair, and eye coloring.
is a rare inherited condition causing reduced pigment and vision problems.
is a genetic condition causing reduced pigment in eyes, skin, and hair.
is an inherited condition causing almost no pigment in skin, hair, eyes.
is an inherited condition causing low pigment in eyes, skin, and hair.
is a genetic condition causing reduced pigment and vision problems.