RS786204430 NEB
Upload your DNA to see your genotype for this variant.
What This Variant Does
"CLNSIG=4
Associated Conditions
Nemaline myopathy 2
Nemaline myopathy
Arthrogryposis multiplex congenita 6
Nemaline myopathy 2
Nemaline myopathy
Arthrogryposis multiplex congenita 6
Other Variants in NEB