ClinVar Miner

Submissions for variant NM_002454.3(MTRR):c.1677-9dup

dbSNP: rs746262908
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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 RCV002183846 SCV002478974 benign Methylcobalamin deficiency type cblE 2024-01-20 criteria provided, single submitter clinical testing

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