ClinVar Miner

Submissions for variant NM_172250.3(MMAA):c.885G>A (p.Leu295=)

dbSNP: rs2126629113
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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 RCV002134357 SCV002453352 likely benign Methylmalonic aciduria, cblA type 2021-03-24 criteria provided, single submitter clinical testing

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