ClinVar Miner

Submissions for variant NM_000297.4(PKD2):c.290_292AGG[7] (p.Glu102dup) (rs750077647)

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Total submissions: 4
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
EGL Genetic Diagnostics,Eurofins Clinical Diagnostics RCV000173103 SCV000224188 likely benign not specified 2014-07-15 criteria provided, single submitter clinical testing
Invitae RCV000200241 SCV000255284 benign Polycystic kidney disease, autosomal dominant 2019-12-31 criteria provided, single submitter clinical testing
Athena Diagnostics Inc RCV000173103 SCV000614572 benign not specified 2017-04-26 criteria provided, single submitter clinical testing
Mendelics RCV000987456 SCV001136751 benign Polycystic kidney disease 2 2019-05-28 criteria provided, single submitter clinical testing

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