ClinVar Miner

Submissions for variant NM_001144967.3(NEDD4L):c.1217A>G (p.His406Arg)

dbSNP: rs2042365082
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Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Labcorp Genetics (formerly Invitae), Labcorp RCV001309431 SCV001498928 likely benign not provided 2022-07-19 criteria provided, single submitter clinical testing
Breakthrough Genomics, Breakthrough Genomics RCV001309431 SCV005193369 uncertain significance not provided criteria provided, single submitter not provided

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