ClinVar Miner

Submissions for variant NM_002835.4(PTPN12):c.860A>G (p.His287Arg)

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Total submissions: 1
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
ARUP Laboratories, Molecular Genetics and Genomics, ARUP Laboratories RCV005233120 SCV005877787 uncertain significance Colorectal cancer 2024-01-30 criteria provided, single submitter clinical testing

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