"GeneDx"[submitter] AND "MAP6"[gene] - ClinVar

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 58916	GRCh38/hg38 11q13.4-13.5(chr11:71928796-77064521)x1	LOC130006424, LOC130006425 +305 more	Copy number loss	See cases	GPathogenic
Select item 58917	GRCh38/hg38 11q13.4-14.1(chr11:71969881-78232895)x1	AAMDC, ACER3 +355 more	Copy number loss	See cases	GPathogenic
Select item 1228318	NC_000011.10:g.75586759C>A	LOC105369391, MAP6	Single nucleotide variant	not provided	GBenign
Select item 1281963	NC_000011.10:g.75586839C>T	LOC105369391, MAP6	Single nucleotide variant	not provided	GBenign
Select item 1289911	NM_033063.2(MAP6):c.1749T>C (p.Asp583=)	LOC105369391, MAP6	Single nucleotide variant (synonymous variant)	not provided	GBenign
Select item 1270127	NM_033063.2(MAP6):c.1120-124C>T	MAP6	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 1223129	NM_033063.2(MAP6):c.741T>G (p.Ile247Met)	MAP6 (I247M)	Single nucleotide variant (missense variant)	not provided	GBenign

ClinVar