ClinVar Miner

Submissions for variant NM_001009944.3(PKD1):c.10221-80del

dbSNP: rs113824832
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Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Molecular Genetics of Inherited Kidney Disorders Laboratory, Garvan Institute of Medical Research RCV001254239 SCV001430231 benign Autosomal dominant polycystic kidney disease 2019-01-01 criteria provided, single submitter research
Department of Pathology and Laboratory Medicine, Sinai Health System RCV001254239 SCV005913886 benign Autosomal dominant polycystic kidney disease 2021-06-16 criteria provided, single submitter clinical testing

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