ClinVar Miner

Submissions for variant NM_203446.3(SYNJ1):c.*741C>T

gnomAD frequency: 0.00001  dbSNP: rs1281984634
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Total submissions: 1
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Labcorp Genetics (formerly Invitae), Labcorp RCV001415574 SCV001617735 likely benign Early-onset Parkinson disease 20; Developmental and epileptic encephalopathy, 53 2022-08-09 criteria provided, single submitter clinical testing

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