RS768434256 COL6A2
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Associated Conditions
Myosclerosis
Ullrich congenital muscular dystrophy 1A
Bethlem myopathy 1A
Inborn genetic diseases
Myosclerosis
Ullrich congenital muscular dystrophy 1A
Bethlem myopathy 1A
Inborn genetic diseases
Other Variants in COL6A2