RS727502829 COL6A2
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What This Variant Does
"CLNSIG=4
Associated Conditions
Collagen 6-related myopathy
Ullrich congenital muscular dystrophy 1A
Bethlem myopathy 1A
Inborn genetic diseases
Collagen 6-related myopathy
Ullrich congenital muscular dystrophy 1A
Bethlem myopathy 1A
Inborn genetic diseases
Other Variants in COL6A2