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Items: 2

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
LAMA2
(F906fs)
Deletion
(frameshift variant)
Merosin deficient congenital muscular dystrophy
GPathogenic
LAMA2
Single nucleotide variant
(intron variant)
Merosin deficient congenital muscular dystrophy
GUncertain significance