"CeGaT Center for Human Genetics Tuebingen"[submitter] AND "KREMEN2"[g - ClinVar

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	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 2646093	NM_172229.3(KREMEN2):c.1032G>A (p.Ala344=)	KREMEN2	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 3024595	GRCh37/hg19 16p13.3(chr16:2990033-4837646)x1	ADCY9, ANKS3 +52 more	Copy number loss	not provided	GPathogenic
Select item 3024594	GRCh37/hg19 16p13.3(chr16:2979687-3220680)x3	BICDL2, CLDN6 +13 more	Copy number gain	not provided	GUncertain significance

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