ClinVar Miner

Submissions for variant NM_015922.3(NSDHL):c.25A>G (p.Met9Val)

gnomAD frequency: 0.00457  dbSNP: rs35529894
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Total submissions: 4
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Genetic Services Laboratory, University of Chicago RCV000146962 SCV000194297 benign not specified 2019-11-29 criteria provided, single submitter clinical testing
Center for Pediatric Genomic Medicine, Children's Mercy Hospital and Clinics RCV000513792 SCV000611026 likely benign not provided 2017-04-17 criteria provided, single submitter clinical testing
Invitae RCV000513792 SCV001019829 benign not provided 2024-01-29 criteria provided, single submitter clinical testing
GeneDx RCV000513792 SCV001905067 benign not provided 2021-02-12 criteria provided, single submitter clinical testing

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