ClinVar Miner

Submissions for variant NM_052867.4(NALCN):c.4104-11del

dbSNP: rs113354194
Minimum review status: Collection method:
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ClinVar version:
Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
GeneDx RCV001556439 SCV001778021 likely benign not provided 2019-07-12 criteria provided, single submitter clinical testing
Labcorp Genetics (formerly Invitae), Labcorp RCV001556439 SCV002965160 benign not provided 2023-12-19 criteria provided, single submitter clinical testing

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