"GeneDx"[submitter] AND "LOC126805999"[gene] - ClinVar

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	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 58116	GRCh38/hg38 1q32.2-44(chr1:209646207-248931113)x3	LOC120908923, LOC120947224 +1352 more	Copy number gain	See cases	GPathogenic
Select item 1285919	NM_000228.3(LAMB3):c.-38+328A>G	LAMB3, LOC126805999	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 1242415	NC_000001.11:g.209652603C>G	LAMB3, LOC126805999	Single nucleotide variant	not provided	GBenign

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