C4310802[trait identifier] AND "OMIM"[submitter] - ClinVar

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	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 253095	NM_001256864.2(DNAJC6):c.2223A>T (p.Thr741=)	DNAJC6	Single nucleotide variant (synonymous variant)	Juvenile onset Parkinson disease 19A	GLikely benign
Select item 253094	NM_001256864.2(DNAJC6):c.2779A>G (p.Arg927Gly)	DNAJC6 (R927G +2 more)	Single nucleotide variant (missense variant)	Parkinson disease 19B, early-onset	GPathogenic