ClinVar Miner

Submissions for variant NM_172250.3(MMAA):c.657C>A (p.Gly219=)

dbSNP: rs1291307841
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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 RCV002219340 SCV002374279 likely benign Methylmalonic aciduria, cblA type 2022-03-15 criteria provided, single submitter clinical testing

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