ClinVar Miner

Submissions for variant NM_000345.4(SNCA):c.9A>G (p.Val3=)

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Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
CeGaT Center for Human Genetics Tuebingen RCV003439415 SCV004152977 likely benign not provided 2022-11-01 criteria provided, single submitter clinical testing SNCA: BP4, BP7
Labcorp Genetics (formerly Invitae), Labcorp RCV003778429 SCV004605290 likely benign Lewy body dementia; Autosomal dominant Parkinson disease 1 2023-03-19 criteria provided, single submitter clinical testing

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