ClinVar Miner

Submissions for variant NM_001044.5(SLC6A3):c.1599+13G>A

gnomAD frequency: 0.00001  dbSNP: rs763612604
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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 RCV002219609 SCV002378285 likely benign Parkinsonism-dystonia, infantile 2022-08-23 criteria provided, single submitter clinical testing

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