RS886042883 COL6A3
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What This Variant Does
"CLNSIG=5
Associated Conditions
Bethlem myopathy 1A
Bethlem myopathy 1A
Inborn genetic diseases
Ullrich congenital muscular dystrophy 1A
Bethlem myopathy 1A
Bethlem myopathy 1A
Inborn genetic diseases
Ullrich congenital muscular dystrophy 1A
Other Variants in COL6A3