ClinVar Miner

Submissions for variant NM_052867.4(NALCN):c.4446+15T>C

gnomAD frequency: 0.00484  dbSNP: rs78312347
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Total submissions: 3
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Center for Pediatric Genomic Medicine, Children's Mercy Hospital and Clinics RCV000515095 SCV000610559 likely benign not provided 2017-04-27 criteria provided, single submitter clinical testing
GeneDx RCV000515095 SCV001765349 likely benign not provided 2018-07-27 criteria provided, single submitter clinical testing
Labcorp Genetics (formerly Invitae), Labcorp RCV000515095 SCV003484249 benign not provided 2025-01-30 criteria provided, single submitter clinical testing

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