"Diagnostic Laboratory, Department of Genetics, University Medical Cen - ClinVar

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	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 808518	NM_014727.3(KMT2B):c.2268_2279dup (p.Gln759_Pro762dup)	KMT2B	Duplication (inframe_insertion)	KMT2B-related disorder +1 more	GConflicting classifications of pathogenicity
Select item 1174896	NM_014727.3(KMT2B):c.5792C>T (p.Pro1931Leu)	KMT2B (P1931L)	Single nucleotide variant (missense variant)	Inborn genetic diseases +1 more	GLikely benign