ClinVar Miner

Submissions for variant NM_153614.4(DNAJB13):c.69-28A>C

gnomAD frequency: 0.43980  dbSNP: rs10793069
Minimum review status: Collection method:
Minimum conflict level:
ClinVar version:
Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
GeneDx RCV001680567 SCV001898244 benign not provided 2018-11-27 criteria provided, single submitter clinical testing
Breakthrough Genomics, Breakthrough Genomics RCV001680567 SCV005232275 benign not provided criteria provided, single submitter not provided

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