RS771336246 NMNAT1
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Associated Conditions
Retinal dystrophy
Leber congenital amaurosis 9
Spondyloepiphyseal dysplasia
sensorineural hearing loss
impaired intellectual development
and leber congenital amaurosis
Retinal dystrophy
Leber congenital amaurosis 9
Spondyloepiphyseal dysplasia
sensorineural hearing loss
impaired intellectual development
and leber congenital amaurosis
Other Variants in NMNAT1