ClinVar Miner

List of variants reported as pathogenic for juvenile-onset Parkinson disease by Fulgent Genetics, Fulgent 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.3057del (p.Tyr1020fs)	rs765632065	0.00007
NM_022089.4(ATP13A2):c.1903C>T (p.Gln635Ter)	rs773246271	0.00003

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