ClinVar Miner

Submissions for variant NM_015629.4(PRPF31):c.1074-8_1074-7del

dbSNP: rs1422807866
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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) RCV001573047 SCV001798349 likely benign not provided no assertion criteria provided clinical testing
Clinical Genetics DNA and cytogenetics Diagnostics Lab, Erasmus MC, Erasmus Medical Center RCV001573047 SCV001963940 likely benign not provided no assertion criteria provided clinical testing

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