ClinVar Miner

Submissions for variant NM_001009944.3(PKD1):c.6621C>G (p.Pro2207=)

dbSNP: rs575553075
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Total submissions: 3
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Preventiongenetics, part of Exact Sciences RCV000250593 SCV000305767 likely benign not specified criteria provided, single submitter clinical testing
Athena Diagnostics Inc RCV000992591 SCV001144995 benign not provided 2018-11-27 criteria provided, single submitter clinical testing
ARUP Laboratories, Molecular Genetics and Genomics, ARUP Laboratories RCV001000838 SCV001157908 likely benign Polycystic kidney disease, adult type 2019-06-18 criteria provided, single submitter clinical testing

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