RS56035053 LAMA2
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Associated Conditions
Merosin deficient congenital muscular dystrophy
LAMA2-related muscular dystrophy
Congenital muscular dystrophy due to partial LAMA2 deficiency
Intellectual disability
Inborn genetic diseases
Limb-girdle muscular dystrophy
Merosin deficient congenital muscular dystrophy
LAMA2-related muscular dystrophy
Congenital muscular dystrophy due to partial LAMA2 deficiency
Intellectual disability
Inborn genetic diseases
Limb-girdle muscular dystrophy
Other Variants in LAMA2