"GeneDx"[submitter] AND "MAP2K7"[gene] - ClinVar

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	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 59082	GRCh38/hg38 19p13.3-13.2(chr19:1972245-9648879)x3	LOC130063254, LOC130063255 +810 more	Copy number gain	See cases	GPathogenic
Select item 1243653	NM_145185.4(MAP2K7):c.856-19T>C	MAP2K7	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 1222270	NM_145185.4(MAP2K7):c.856-8C>G	MAP2K7	Single nucleotide variant (intron variant)	not provided	GBenign

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