RS794727136 NEB

Health Risk Chr 2:151493781
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What This Variant Does
"CLNSIG=5
Associated Conditions
Nemaline myopathy 2
Inborn genetic diseases
Nemaline myopathy 2
Arthrogryposis multiplex congenita 6
Nemaline myopathy 2
Inborn genetic diseases
Nemaline myopathy 2
Arthrogryposis multiplex congenita 6
Other Variants in NEB
rs1057515573 rs1057515574 rs2551726621 rs121913662 rs1057515575 rs200545007 rs398124167 rs117178114 rs182847302 rs201189784
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