ClinVar Miner

Submissions for variant NM_000338.3(SLC12A1):c.2043-9dup

dbSNP: rs112495679
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Total submissions: 4
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
PreventionGenetics, part of Exact Sciences RCV000244143 SCV000303693 benign not specified criteria provided, single submitter clinical testing
Athena Diagnostics RCV000713320 SCV000843916 benign not provided 2018-08-15 criteria provided, single submitter clinical testing
Labcorp Genetics (formerly Invitae), Labcorp RCV000713320 SCV001724603 benign not provided 2025-02-03 criteria provided, single submitter clinical testing
GeneDx RCV000713320 SCV001872127 benign not provided 2020-02-03 criteria provided, single submitter clinical testing

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