RS201734774 NEB

Health Risk Chr 2:151570579
Upload your DNA to see your genotype for this variant.
Associated Conditions
Nemaline myopathy 2
Inborn genetic diseases
Congenital structural myopathy
Nemaline myopathy 2
Inborn genetic diseases
Congenital structural myopathy
Other Variants in NEB
rs1057515573 rs1057515574 rs2551726621 rs121913662 rs1057515575 rs200545007 rs398124167 rs117178114 rs182847302 rs201189784
Ask Dr. Hemsworth about this variant