ClinVar Miner

Submissions for variant NM_203446.3(SYNJ1):c.*770C>T

dbSNP: rs2039298283
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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 RCV001070167 SCV001235383 uncertain significance Early-onset Parkinson disease 20; Developmental and epileptic encephalopathy, 53 2021-09-01 criteria provided, single submitter clinical testing

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