ClinVar Miner

Submissions for variant NM_017986.4(SLC52A1):c.189G>C (p.Leu63=)

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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 RCV005098859 SCV003473759 likely benign not provided 2022-03-01 criteria provided, single submitter clinical testing

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