ClinVar Miner

Submissions for variant NM_001044.5(SLC6A3):c.1157-20C>G

dbSNP: rs2126344195
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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 RCV002073893 SCV002426753 likely benign Parkinsonism-dystonia, infantile 2021-11-01 criteria provided, single submitter clinical testing

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