ClinVar Miner

Submissions for variant NM_148960.3(CLDN19):c.277G>A (p.Val93Met)

gnomAD frequency: 0.00063  dbSNP: rs34374110
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Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Labcorp Genetics (formerly Invitae), Labcorp RCV000901929 SCV001046325 likely benign not provided 2024-12-07 criteria provided, single submitter clinical testing
GeneDx RCV000901929 SCV005414671 uncertain significance not provided 2024-05-24 criteria provided, single submitter clinical testing In silico analysis indicates that this missense variant does not alter protein structure/function; Has not been previously published as pathogenic or benign to our knowledge

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