"Diagnostic Laboratory, Department of Genetics, University Medical Cen - ClinVar

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	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 1049330	NM_001448.3(GPC4):c.772C>T (p.Arg258Trp)	GPC4 (R258W)	Single nucleotide variant (missense variant)	Inborn genetic diseases +1 more	GConflicting classifications of pathogenicity
Select item 1299875	NM_001448.3(GPC4):c.38T>A (p.Leu13Gln)	GPC4 (L13Q)	Single nucleotide variant (missense variant)	GPC4-related disorder	GLikely benign