ClinVar Miner

Submissions for variant NM_000254.3(MTR):c.1696-18T>C

dbSNP: rs2103252601
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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 RCV002078256 SCV002377925 likely benign Methylcobalamin deficiency type cblG 2021-08-11 criteria provided, single submitter clinical testing

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