ClinVar Miner

Submissions for variant NM_000355.4(TCN2):c.941-21G>A

gnomAD frequency: 0.12200  dbSNP: rs2283873
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Total submissions: 3
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
GeneDx RCV001598058 SCV001830390 benign not provided 2018-07-31 criteria provided, single submitter clinical testing
Labcorp Genetics (formerly Invitae), Labcorp RCV003598052 SCV004450465 benign Transcobalamin II deficiency 2022-12-24 criteria provided, single submitter clinical testing
Breakthrough Genomics, Breakthrough Genomics RCV001598058 SCV005274021 benign not provided criteria provided, single submitter not provided

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