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 genetic disorder causing conductive hearing loss, droopy eyelids, and bone differences.
is an inherited retinal disorder causing central vision loss and color problems.
is an inherited retinal disorder causing daytime vision loss and night blindness.
is a genetic retinal disorder causing progressive central vision and color loss.
is an inherited eye disorder causing progressive cone then rod vision loss.
is an inherited retinal disease causing progressive central and color vision loss.
is an inherited eye disorder causing daylight and later night vision loss.
is a rare inherited eye disorder causing worsening central and color vision.
is a genetic eye disorder causing progressive vision loss and color problems.
is an inherited retinal disorder causing progressive vision and color loss.
is an inherited retinal disorder causing progressive color and central vision loss.
is an inherited eye disorder damaging cone and rod cells, impairing vision.
is an inherited retinal disorder causing progressive central and color vision loss.
is an inherited retinal disease causing progressive central vision loss and photosensitivity.
is a rare inherited retinal disease causing color and night vision loss.
is an inherited retinal disorder causing progressive vision loss and color problems.
is a genetic eye disease causing progressive cone and rod cell damage.
is a genetic eye disorder causing progressive vision loss and light sensitivity.
is a genetic retinal disorder causing progressive color and central vision loss.
is a genetic retinal condition causing progressive central, color, and night-vision loss.
is a rare macular disorder causing progressive central vision loss.