ClinVar Miner

Submissions for variant NM_000355.4(TCN2):c.879G>T (p.Leu293=)

dbSNP: rs777393779
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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 RCV001435302 SCV001638121 likely benign Transcobalamin II deficiency 2020-10-19 criteria provided, single submitter clinical testing

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