ClinVar Miner

Submissions for variant NM_006904.7(PRKDC):c.324+193G>T

dbSNP: rs13277684
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 RCV001658739 SCV001872975 benign not provided 2019-08-06 criteria provided, single submitter clinical testing
Breakthrough Genomics, Breakthrough Genomics RCV001658739 SCV005265553 benign not provided criteria provided, single submitter not provided

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