List of variants in gene SYNJ1 reported as likely pathogenic for Early-onset Parkinson disease 20; Developmental and epileptic encephalopathy, 53

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: 8

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HGVS	dbSNP	gnomAD frequency
NM_203446.3(SYNJ1):c.1201-2A>G	rs1569086116	0.00001
NC_000021.8:g.(?_34029319)_(34031816_?)del
NM_203446.3(SYNJ1):c.2461+2T>C	rs2517541465
NM_203446.3(SYNJ1):c.3247+2T>G	rs2517442308
NM_203446.3(SYNJ1):c.3430+1G>A	rs2145769010
NM_203446.3(SYNJ1):c.3478+1G>A	rs1085307987
NM_203446.3(SYNJ1):c.3589-1G>A	rs2517368826
NM_203446.3(SYNJ1):c.789+1G>A	rs2042124608

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