ClinVar Miner

List of variants reported as uncertain significance for autosomal recessive juvenile Parkinson disease 2 by Genetics and Molecular Pathology, SA Pathology

Included ClinVar conditions (4):

Minimum submission review status:		Collection method:
Minimum conflict level: Report conflict between different conditions
Show significances as they were submitted (without aggregation into standard terms)
		ClinVar version:

Total variants: 2

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HGVS	dbSNP	gnomAD frequency
NM_004562.3(PRKN):c.744C>G (p.Val248=)	rs771437898	0.00006
NM_004562.3(PRKN):c.904C>T (p.His302Tyr)	rs755749488	0.00001

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