ClinVar Miner

Submissions for variant NM_001008537.3(NEXMIF):c.1998AGA[1] (p.Glu667del)

dbSNP: rs764439412
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Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Genetic Services Laboratory, University of Chicago RCV000194278 SCV000247699 uncertain significance not specified 2014-12-18 criteria provided, single submitter clinical testing
Labcorp Genetics (formerly Invitae), Labcorp RCV001516594 SCV001724894 benign not provided 2023-12-13 criteria provided, single submitter clinical testing

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