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Items: 2

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
LAMA1
(G2899fs)
Duplication
(frameshift variant)
LAMA1-related disorder
GPathogenic
LAMA1, LOC112543434
Single nucleotide variant
(intron variant)
LAMA1-related disorder
GPathogenic