Related gene-specific medical variations for Gene (Select 4300) - ClinVar

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 3396838	NM_004529.4(MLLT3):c.65A>G (p.Lys22Arg)	LOC130001579, MLLT3 (K19R +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3063068	GRCh37/hg19 9p21.3(chr9:20373651-20571020)x1	MLLT3	Copy number loss	not specified	GUncertain significance
Select item 2685343	GRCh37/hg19 9p21.3(chr9:20194314-20369546)x1	MLLT3	Copy number loss	not provided	GUncertain significance
Select item 1527511	GRCh37/hg19 9p21.3(chr9:20407662-20489380)	MLLT3	Copy number loss	not specified	GUncertain significance
Select item 1527510	GRCh37/hg19 9p21.3(chr9:20194313-20364684)	MLLT3	Copy number loss	not specified	GUncertain significance
Select item 688950	GRCh37/hg19 9p21.3(chr9:20323068-20457595)x1	MLLT3	Copy number loss	not provided	GUncertain significance
Select item 394964	GRCh37/hg19 9p21.3(chr9:19942083-20445889)x3	MLLT3	Copy number gain	See cases	GLikely benign

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