ClinVar Miner

Submissions for variant NM_002467.6(MYC):c.64T>C (p.Phe22Leu)

gnomAD frequency: 0.00222  dbSNP: rs146505192
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Total submissions: 3
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Labcorp Genetics (formerly Invitae), Labcorp RCV000896531 SCV001040627 benign not provided 2018-06-14 criteria provided, single submitter clinical testing
CeGaT Center for Human Genetics Tuebingen RCV000896531 SCV004163209 likely benign not provided 2023-01-01 criteria provided, single submitter clinical testing MYC: BP4, BS2
Breakthrough Genomics, Breakthrough Genomics RCV000896531 SCV005270838 benign not provided criteria provided, single submitter not provided

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