ClinVar Miner

Submissions for variant NM_001008537.3(NEXMIF):c.1154G>A (p.Gly385Asp)

dbSNP: rs375109305
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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 RCV001370023 SCV001566484 benign not provided 2024-02-12 criteria provided, single submitter clinical testing
GeneDx RCV001370023 SCV002001261 likely benign not provided 2020-12-18 criteria provided, single submitter clinical testing

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