ClinVar Miner

Submissions for variant NM_000355.4(TCN2):c.858T>G (p.Ala286=)

dbSNP: rs988793927
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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 RCV003598013 SCV001121534 likely benign Transcobalamin II deficiency 2023-04-25 criteria provided, single submitter clinical testing

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