Related gene-specific medical variations for Gene (Select 8685) - ClinVar

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	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 2599915	NM_006770.4(MARCO):c.1295G>A (p.Arg432Gln)	LOC126806328, MARCO (R432Q)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2383961	NM_006770.4(MARCO):c.1348G>A (p.Glu450Lys)	LOC126806328, MARCO (E450K)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 1340755	GRCh37/hg19 2q14.2(chr2:119661412-119751867)x1	MARCO	Copy number loss	not provided	GUncertain significance

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