ClinVar Miner

List of variants reported as likely pathogenic for juvenile-onset Parkinson disease by Baylor Genetics

Included ClinVar conditions (7):

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_022089.4(ATP13A2):c.943G>A (p.Gly315Arg)	rs150519745	0.00005
NM_022089.4(ATP13A2):c.2529+1G>A	rs776448394	0.00001

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