ClinVar Miner

Submissions for variant NM_145261.4(DNAJC19):c.4-128_4-127insG

gnomAD frequency: 0.01035  dbSNP: rs766807321
Minimum review status: Collection method:
Minimum conflict level:
ClinVar version:
Total submissions: 1
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
GeneDx RCV001587488 SCV001814386 likely benign not provided 2019-08-10 criteria provided, single submitter clinical testing

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