ClinVar Miner

Submissions for variant NM_001009944.3(PKD1):c.8705A>G (p.Gln2902Arg)

dbSNP: rs1400163523
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Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Greenwood Genetic Center Diagnostic Laboratories, Greenwood Genetic Center RCV002280314 SCV002568345 uncertain significance not provided 2022-05-09 criteria provided, single submitter clinical testing PM2, BP4
Fulgent Genetics, Fulgent Genetics RCV005008514 SCV005640854 uncertain significance Polycystic kidney disease, adult type 2024-05-17 criteria provided, single submitter clinical testing

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