ClinVar Miner

Submissions for variant NM_000355.4(TCN2):c.581-9dup

dbSNP: rs2145544145
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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 RCV002136703 SCV002405463 benign Transcobalamin II deficiency 2021-02-16 criteria provided, single submitter clinical testing

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