ClinVar Miner

List of variants in gene GBA1 reported as uncertain significance for synucleinopathy

Included ClinVar conditions (15):

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)
		ClinVar version:

Total variants: 2

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HGVS	dbSNP	gnomAD frequency
NM_000157.4(GBA1):c.104C>T (p.Ser35Leu)	rs757041827	0.00001
NM_000157.4(GBA1):c.10T>C (p.Ser4Pro)	rs2148083300

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