"PreventionGenetics, part of Exact Sciences"[submitter] AND "PLEKHG6"[ - ClinVar

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	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 3038576	NM_001384598.1(PLEKHG6):c.139-457del	PLEKHG6	Deletion (5 prime UTR variant +1 more)	PLEKHG6-related disorder	GBenign
Select item 3061591	NM_001384598.1(PLEKHG6):c.756+2T>C	PLEKHG6	Single nucleotide variant (splice donor variant)	PLEKHG6-related disorder	GUncertain significance
Select item 3035059	NM_001384598.1(PLEKHG6):c.1825C>T (p.Arg609Cys)	PLEKHG6 (R495C +4 more)	Single nucleotide variant (missense variant +1 more)	PLEKHG6-related disorder	GLikely benign

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