ClinVar Miner

Submissions for variant NM_014633.5(CTR9):c.2313T>C (p.Asp771=)

gnomAD frequency: 0.00116  dbSNP: rs138718780
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ClinVar version:
Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Labcorp Genetics (formerly Invitae), Labcorp RCV001516246 SCV001724503 benign not provided 2024-02-25 criteria provided, single submitter clinical testing
GeneDx RCV001516246 SCV002004360 likely benign not provided 2021-03-31 criteria provided, single submitter clinical testing

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