ClinVar Miner

Submissions for variant NM_014208.3(DSPP):c.3695A>G (p.Asn1232Ser)

dbSNP: rs111876111
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Total submissions: 4
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
GeneDx RCV001573208 SCV001882621 benign not provided 2018-11-29 criteria provided, single submitter clinical testing
Breakthrough Genomics, Breakthrough Genomics RCV001573208 SCV005303283 benign not provided criteria provided, single submitter not provided
Laboratory of Diagnostic Genome Analysis, Leiden University Medical Center (LUMC) RCV001573208 SCV001798715 likely benign not provided no assertion criteria provided clinical testing
Clinical Genetics DNA and cytogenetics Diagnostics Lab, Erasmus MC, Erasmus Medical Center RCV001573208 SCV001965342 likely benign not provided no assertion criteria provided clinical testing

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