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Items: 2

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
LAMA2
(G2589fs +1 more)
Deletion
(frameshift variant)
Merosin deficient congenital muscular dystrophy
GPathogenic
LAMA2
(R2790fs +1 more)
Deletion
(frameshift variant)
Merosin deficient congenital muscular dystrophy
GPathogenic