ClinVar Miner

Submissions for variant NM_001009944.3(PKD1):c.10051-25G>A

gnomAD frequency: 0.00935  dbSNP: rs150399422
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Total submissions: 3
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
ARUP Laboratories, Molecular Genetics and Genomics, ARUP Laboratories RCV000508326 SCV000604731 benign Polycystic kidney disease, adult type 2019-08-15 criteria provided, single submitter clinical testing
Molecular Genetics of Inherited Kidney Disorders Laboratory, Garvan Institute of Medical Research RCV001254313 SCV001430265 benign Autosomal dominant polycystic kidney disease 2019-01-01 criteria provided, single submitter research
Breakthrough Genomics, Breakthrough Genomics RCV004715247 SCV005290680 benign not provided criteria provided, single submitter not provided

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