ClinVar Miner

Submissions for variant NM_015268.4(DNAJC13):c.3942G>A (p.Pro1314=)

gnomAD frequency: 0.00494  dbSNP: rs35658317
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Minimum conflict level:
ClinVar version:
Total submissions: 4
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Labcorp Genetics (formerly Invitae), Labcorp RCV000881123 SCV001024268 benign not provided 2019-12-31 criteria provided, single submitter clinical testing
Breakthrough Genomics, Breakthrough Genomics RCV000881123 SCV005300019 benign not provided criteria provided, single submitter not provided
Genome Diagnostics Laboratory, Amsterdam University Medical Center RCV000881123 SCV001808925 likely benign not provided no assertion criteria provided clinical testing
Clinical Genetics DNA and cytogenetics Diagnostics Lab, Erasmus MC, Erasmus Medical Center RCV000881123 SCV001968583 likely benign not provided no assertion criteria provided clinical testing

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