ClinVar Miner

Submissions for variant NM_000273.3(GPR143):c.677del (p.Gly226fs)

dbSNP: rs281865182
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Total submissions: 3
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Retina International RCV000084938 SCV000117074 not provided not provided no assertion provided not provided
Clinical Genetics, Academic Medical Center RCV000084938 SCV002034348 pathogenic not provided no assertion criteria provided clinical testing
Joint Genome Diagnostic Labs from Nijmegen and Maastricht, Radboudumc and MUMC+ RCV000084938 SCV002037268 pathogenic not provided no assertion criteria provided clinical testing

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