"Fulgent Genetics, Fulgent Genetics"[submitter] AND "LOC126859871"[gen - ClinVar

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	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 41223	NM_004562.3(PRKN):c.500G>A (p.Ser167Asn)	LOC126859871, PRKN (S167N)	Single nucleotide variant (missense variant +1 more)	not provided +4 more	GBenign/Likely benign
Select item 468587	NM_004562.3(PRKN):c.458C>G (p.Pro153Arg)	PRKN, LOC126859871 (P153R)	Single nucleotide variant (missense variant +1 more)	not provided +3 more	GBenign/Likely benign