ClinVar Miner

Submissions for variant NM_001008537.3(NEXMIF):c.3361C>T (p.Arg1121Trp)

gnomAD frequency: 0.00008  dbSNP: rs199579887
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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 RCV001511748 SCV001719044 benign not provided 2024-06-15 criteria provided, single submitter clinical testing
GeneDx RCV001511748 SCV001982175 likely benign not provided 2021-03-19 criteria provided, single submitter clinical testing

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