ClinVar Miner

Submissions for variant NM_015268.4(DNAJC13):c.2550-9A>T

gnomAD frequency: 0.61432  dbSNP: rs2369796
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Total submissions: 4
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
GeneDx RCV001673223 SCV001885086 benign not provided 2018-07-05 criteria provided, single submitter clinical testing
Breakthrough Genomics, Breakthrough Genomics RCV001673223 SCV005300008 benign not provided criteria provided, single submitter not provided
Genome Diagnostics Laboratory, Amsterdam University Medical Center RCV001579831 SCV001808660 benign not specified no assertion criteria provided clinical testing
Clinical Genetics DNA and cytogenetics Diagnostics Lab, Erasmus MC, Erasmus Medical Center RCV001579831 SCV001967077 benign not specified no assertion criteria provided clinical testing

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