List of variants in gene SYNJ1 reported as likely pathogenic for Early-onset Parkinson disease 20

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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: 3

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HGVS	dbSNP	gnomAD frequency
NM_203446.3(SYNJ1):c.2242C>T (p.Gln748Ter)
NM_203446.3(SYNJ1):c.2254del (p.Asp752fs)	rs2040866242
NM_203446.3(SYNJ1):c.2398C>T (p.Arg800Cys)

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