ClinVar (all) for Orgtrack (Select 505414) - ClinVar

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	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 424722	NM_014783.5(ARHGAP11A):c.[1355C>G];[932G>T]			Macrocephaly +1 more	GLikely benign
Select item 189393	19p13.12 duplication		Duplication	Macrocephaly +1 more	GLikely pathogenic
Select item 189392	NM_199261.4(TPTE):c.1357-3_1357-2del	TPTE	Deletion (splice acceptor variant)	Macrocephaly +1 more	GUncertain significance

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