ClinVar Miner

Submissions for variant NM_001015880.2(PAPSS2):c.381+21_381+24del

dbSNP: rs367885911
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Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Laboratory of Diagnostic Genome Analysis, Leiden University Medical Center (LUMC) RCV001795689 SCV002035753 likely benign not provided no assertion criteria provided clinical testing
Clinical Genetics DNA and cytogenetics Diagnostics Lab, Erasmus MC, Erasmus Medical Center RCV001796932 SCV002038297 benign not specified no assertion criteria provided clinical testing

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