ClinVar Miner

Submissions for variant NM_001044.5(SLC6A3):c.360C>T (p.Leu120=)

gnomAD frequency: 0.00004  dbSNP: rs148447720
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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 RCV001394824 SCV001596514 likely benign Parkinsonism-dystonia, infantile 2021-10-12 criteria provided, single submitter clinical testing

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