ClinVar Miner

Submissions for variant NM_000316.3(PTH1R):c.1353+17C>T

gnomAD frequency: 0.00143  dbSNP: rs202140438
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Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Labcorp Genetics (formerly Invitae), Labcorp RCV002125037 SCV002407126 benign not provided 2024-01-29 criteria provided, single submitter clinical testing
ARUP Laboratories, Molecular Genetics and Genomics, ARUP Laboratories RCV002125037 SCV004564376 likely benign not provided 2023-05-02 criteria provided, single submitter clinical testing

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