ClinVar Miner

Submissions for variant NM_004247.4(EFTUD2):c.1447A>G (p.Ser483Gly)

dbSNP: rs1597797872
Minimum review status: Collection method:
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ClinVar version:
Total submissions: 1
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Labcorp Genetics (formerly Invitae), Labcorp RCV000880318 SCV001023405 benign not provided 2019-12-31 criteria provided, single submitter clinical testing

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