ClinVar Miner

Submissions for variant NM_000481.4(AMT):c.42C>T (p.Arg14=)

dbSNP: rs2107938326
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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 RCV001442714 SCV001645667 likely benign Glycine encephalopathy 2020-06-21 criteria provided, single submitter clinical testing

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