RS199758082 SPEG

Health Risk Chr 2:219483187
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Associated Conditions
Inborn genetic diseases
Myopathy
centronuclear
5
Inborn genetic diseases
Myopathy
centronuclear
5
Other Variants in SPEG
rs587777672 rs587777673 rs587777674 rs587777675 rs531879999 rs371302780 rs565137573 rs77314619 rs377476081 rs201901718
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