ClinVar Miner

Submissions for variant NM_000355.4(TCN2):c.65-7T>C

gnomAD frequency: 0.00002  dbSNP: rs201199639
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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 RCV003858267 SCV004655026 likely benign Transcobalamin II deficiency 2024-04-14 criteria provided, single submitter clinical testing

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