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Items: 3

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
LAMA4, LOC126859766
(E930G +1 more)
Single nucleotide variant
(missense variant)
not specified
+3 more
GBenign/Likely benign
LAMA4, LOC126859766
(P921T +1 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
LAMA4, LOC126859766
(D913N +1 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
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