ClinVar Miner

Submissions for variant NM_000297.4(PKD2):c.1320-2del

dbSNP: rs1578135823
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Total submissions: 1
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Center For Human Genetics And Laboratory Diagnostics, Dr. Klein, Dr. Rost And Colleagues RCV000790467 SCV000929794 pathogenic Polycystic kidney disease 2 2019-01-21 criteria provided, single submitter clinical testing

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