ClinVar Miner

Submissions for variant NM_032588.4(TRIM63):c.709A>G (p.Lys237Glu)

gnomAD frequency: 0.21674  dbSNP: rs2275950
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ClinVar version:
Total submissions: 3
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
GeneDx RCV001640938 SCV001856644 benign not provided 2018-09-06 criteria provided, single submitter clinical testing
Women's Health and Genetics/Laboratory Corporation of America, LabCorp RCV003230685 SCV003928623 likely benign not specified 2023-04-09 criteria provided, single submitter clinical testing
Breakthrough Genomics, Breakthrough Genomics RCV001640938 SCV005284374 benign not provided criteria provided, single submitter not provided

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