ClinVar Miner

Submissions for variant NM_031475.3(ESPN):c.702C>G (p.Ser234=)

dbSNP: rs367944375
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Total submissions: 5
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
GeneDx RCV000991970 SCV000717130 likely benign not provided 2021-06-03 criteria provided, single submitter clinical testing
Athena Diagnostics RCV000991970 SCV001143885 benign not provided 2018-11-16 criteria provided, single submitter clinical testing
ARUP Laboratories, Molecular Genetics and Genomics, ARUP Laboratories RCV000991970 SCV001474260 benign not provided 2023-11-11 criteria provided, single submitter clinical testing
Labcorp Genetics (formerly Invitae), Labcorp RCV000991970 SCV003261917 benign not provided 2024-12-08 criteria provided, single submitter clinical testing
Breakthrough Genomics, Breakthrough Genomics RCV000991970 SCV005260977 likely benign not provided criteria provided, single submitter not provided

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