ClinVar Miner

Submissions for variant NM_058246.4(DNAJB6):c.*3C>T

gnomAD frequency: 0.00019  dbSNP: rs140445215
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
Eurofins Ntd Llc (ga) RCV000339060 SCV000333333 uncertain significance not provided 2018-09-14 criteria provided, single submitter clinical testing
Breakthrough Genomics, Breakthrough Genomics RCV000339060 SCV005195757 uncertain significance not provided criteria provided, single submitter not provided

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