RS549794342 NEB
Upload your DNA to see your genotype for this variant.
What This Variant Does
"CLNSIG=4
Associated Conditions
Limb pain
Progressive proximal muscle weakness
Muscular dystrophy
Nemaline myopathy 2
Arthrogryposis multiplex congenita 6
Nemaline myopathy
NEB-related disorder
Limb pain
Progressive proximal muscle weakness
Muscular dystrophy
Nemaline myopathy 2
Arthrogryposis multiplex congenita 6
Nemaline myopathy
NEB-related disorder
Other Variants in NEB