ClinVar Miner

Submissions for variant NM_014251.3(SLC25A13):c.333T>C (p.Asp111=)

dbSNP: rs1349801909
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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 RCV000928879 SCV001074500 likely benign Citrin deficiency 2022-03-17 criteria provided, single submitter clinical testing

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