ClinVar Miner

Submissions for variant NM_203446.3(SYNJ1):c.1510+13T>A

dbSNP: rs75688000
Minimum review status: Collection method:
Minimum conflict level:
Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Breakthrough Genomics, Breakthrough Genomics RCV004718996 SCV005307697 benign not provided criteria provided, single submitter not provided
Labcorp Genetics (formerly Invitae), Labcorp RCV002115756 SCV002409813 benign Early-onset Parkinson disease 20; Developmental and epileptic encephalopathy, 53 2026-02-04 criteria provided, single submitter clinical testing

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