ClinVar Miner

List of variants reported as not provided for synucleinopathy

Included ClinVar conditions (15):

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: 3

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HGVS	dbSNP	gnomAD frequency
NM_000157.4(GBA1):c.1226A>G (p.Asn409Ser)	rs76763715	0.00191
NM_003085.5(SNCB):c.368C>A (p.Pro123His)	rs104893937	0.00021
GRCh37/hg19 4q22.1(chr4:90647779-90756863)x3

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