ClinVar Miner

Submissions for variant NM_006904.6(PRKDC):c.10626C>T (p.Phe3542=) (rs8178231)

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Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
GeneDx RCV001712213 SCV000518592 likely benign not provided 2018-04-23 criteria provided, single submitter clinical testing
Invitae RCV000551744 SCV000655358 benign Immunodeficiency 26 with or without neurologic abnormalities 2020-11-27 criteria provided, single submitter clinical testing

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