"Genome Diagnostics Laboratory, University Medical Center Utrecht"[sub - ClinVar

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	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 337834	NM_024411.5(PDYN):c.600T>C (p.His200=)	PDYN, PDYN-AS1	Single nucleotide variant (synonymous variant)	not provided +2 more	GBenign
Select item 337839	NM_024411.5(PDYN):c.436A>C (p.Met146Leu)	PDYN-AS1, PDYN (M146L)	Single nucleotide variant (missense variant)	not specified +2 more	GBenign/Likely benign
Select item 1284957	NM_024411.5(PDYN):c.74G>A (p.Arg25Gln)	PDYN, PDYN-AS1 (R25Q)	Single nucleotide variant (missense variant)	not provided	GUncertain significance

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ClinVar