ClinVar Miner

Submissions for variant NM_001384140.1(PCDH15):c.189A>G (p.Lys63=)

dbSNP: rs1554940478
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Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Eurofins Ntd Llc (ga) RCV000597217 SCV000703507 uncertain significance not provided 2016-12-12 criteria provided, single submitter clinical testing
Labcorp Genetics (formerly Invitae), Labcorp RCV000597217 SCV002348117 likely benign not provided 2023-03-11 criteria provided, single submitter clinical testing

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