"VPS11-related disorder"[Disease/phenotype] AND "PreventionGenetics, p - ClinVar

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	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 784205	NM_021729.6(VPS11):c.87C>T (p.Pro29=)	VPS11	Single nucleotide variant (5 prime UTR variant +2 more)	not provided +1 more	GBenign/Likely benign
Select item 3040830	NM_021729.6(VPS11):c.187+92G>C	VPS11 (A12P)	Single nucleotide variant (missense variant +1 more)	VPS11-related disorder	GBenign
Select item 2642455	NM_021729.6(VPS11):c.2301A>G (p.Thr767=)	VPS11	Single nucleotide variant (synonymous variant +1 more)	VPS11-related disorder +1 more	GLikely benign

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