"PreventionGenetics, part of Exact Sciences"[submitter] AND "GPC5"[gen - ClinVar

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	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 3046562	NM_004466.6(GPC5):c.557G>T (p.Ser186Ile)	GPC5 (S186I)	Single nucleotide variant (missense variant)	GPC5-related disorder	GLikely benign
Select item 3041123	NM_004466.6(GPC5):c.730T>G (p.Phe244Val)	GPC5 (F244V)	Single nucleotide variant (missense variant)	GPC5-related disorder	GLikely benign
Select item 3054299	NM_004466.6(GPC5):c.776C>G (p.Pro259Arg)	GPC5 (P259R)	Single nucleotide variant (missense variant)	GPC5-related disorder	GLikely benign

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