ClinVar Miner

Submissions for variant NM_006904.7(PRKDC):c.9337-6_9337-4del

dbSNP: rs11311765
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
Invitae RCV000894190 SCV001038160 benign not provided 2017-08-10 criteria provided, single submitter clinical testing
GeneDx RCV000894190 SCV002027705 likely benign not provided 2021-05-17 criteria provided, single submitter clinical testing

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