ClinVar Miner

Submissions for variant NM_001009944.3(PKD1):c.11661del (p.Phe3888fs)

dbSNP: rs2151695275
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Total submissions: 1
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Molecular Diagnostics Laboratory, M Health Fairview: University of Minnesota RCV001731130 SCV001981543 likely pathogenic Polycystic kidney disease, adult type 2021-08-25 criteria provided, single submitter clinical testing

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