RS202057799 NMNAT1

Health Risk Chr 1:9982354
Upload your DNA to see your genotype for this variant.
Associated Conditions
Leber congenital amaurosis 9
Inborn genetic diseases
NMNAT1-related disorder
Spondyloepiphyseal dysplasia
sensorineural hearing loss
impaired intellectual development
and leber congenital amaurosis
Leber congenital amaurosis 9
Inborn genetic diseases
NMNAT1-related disorder
Spondyloepiphyseal dysplasia
sensorineural hearing loss
impaired intellectual development
and leber congenital amaurosis
Other Variants in NMNAT1
rs387907290 rs142968179 rs150726175 rs387907291 rs368062092 rs387907293 rs387907294 rs748902766 rs138613460 rs371526758
Ask Dr. Hemsworth about this variant