ClinVar Miner

Submissions for variant NM_001009944.3(PKD1):c.12138+5G>A

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Total submissions: 1
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Department of Pathology and Laboratory Medicine, Sinai Health System RCV005362383 SCV005913974 uncertain significance Autosomal dominant polycystic kidney disease 2023-04-13 criteria provided, single submitter clinical testing

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