ClinVar Miner

Submissions for variant NM_000481.4(AMT):c.12T>A (p.Ala4=)

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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 RCV003043610 SCV003345297 likely benign Glycine encephalopathy 2022-05-21 criteria provided, single submitter clinical testing

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