"GeneDx"[submitter] AND "MAGI1"[gene] - ClinVar - NCBI

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Items: 4

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 57772	GRCh38/hg38 3p14.1-12.3(chr3:64761248-78410098)x1	ADAMTS9-AS2, ARL6IP5 +234 more	Copy number loss	See cases	GPathogenic
Select item 380114	NM_001033057.2(MAGI1):c.1123A>G (p.Ile375Val)	MAGI1 (I375V +1 more)	Single nucleotide variant (missense variant)	not specified +1 more	GLikely benign
Select item 151736	GRCh38/hg38 3p14.1(chr3:65536355-65582844)x3	MAGI1	Copy number gain	See cases	GLikely benign
Select item 253801	GRCh37/hg19 3p14.1(chr3:65634239-66656496)x3	LRIG1, MAGI1	Copy number gain	See cases	GUncertain significance

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