ClinVar Miner

Submissions for variant NM_005204.4(MAP3K8):c.234T>C (p.Tyr78=)

gnomAD frequency: 0.45386  dbSNP: rs1042058
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Total submissions: 5
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
GeneDx RCV001537203 SCV001754057 benign not provided 2018-09-04 criteria provided, single submitter clinical testing
Labcorp Genetics (formerly Invitae), Labcorp RCV001537203 SCV002402586 benign not provided 2025-02-03 criteria provided, single submitter clinical testing
Breakthrough Genomics, Breakthrough Genomics RCV001537203 SCV005317035 benign not provided criteria provided, single submitter not provided
Diagnostic Laboratory, Department of Genetics, University Medical Center Groningen RCV001528717 SCV001740928 benign not specified no assertion criteria provided clinical testing
Genome Diagnostics Laboratory, Amsterdam University Medical Center RCV001528717 SCV001807267 benign not specified no assertion criteria provided clinical testing

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