ClinVar Miner

List of variants in gene PRKN reported as likely pathogenic for Autosomal recessive juvenile Parkinson disease 2; Ovarian neoplasm; Lung cancer

Minimum submission review status:		Collection method:
Minimum conflict level: Report conflict between different conditions
Gene type: Distinguish antisense genes from sense genes
Show significances as they were submitted (without aggregation into standard terms)
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Total variants: 2

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HGVS	dbSNP	gnomAD frequency
NM_004562.3(PRKN):c.98G>A (p.Arg33Gln)	rs147757966	0.00006
NM_004562.3(PRKN):c.73C>T (p.Gln25Ter)	rs1440010564

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