ClinVar Miner

Submissions for variant NM_058004.4(PI4KA):c.42_53del (p.Gly15_Gly18del)

dbSNP: rs551553536
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Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Labcorp Genetics (formerly Invitae), Labcorp RCV000972991 SCV001120724 benign not provided 2019-12-31 criteria provided, single submitter clinical testing
Genetic Services Laboratory, University of Chicago RCV001819129 SCV002064920 likely benign not specified 2019-07-22 criteria provided, single submitter clinical testing

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