ClinVar Miner

Submissions for variant NM_172250.3(MMAA):c.439+1G>A

dbSNP: rs1553957938
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Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Counsyl RCV000674400 SCV000799729 likely pathogenic Methylmalonic aciduria, cblA type 2018-05-03 criteria provided, single submitter clinical testing
Baylor Genetics RCV000674400 SCV004193121 likely pathogenic Methylmalonic aciduria, cblA type 2022-12-31 criteria provided, single submitter clinical testing

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