ClinVar Miner

Submissions for variant NM_001384140.1(PCDH15):c.3410A>G (p.Glu1137Gly)

dbSNP: rs1439470139
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Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Women's Health and Genetics/Laboratory Corporation of America, LabCorp RCV004587101 SCV005077065 uncertain significance not specified 2024-04-22 criteria provided, single submitter clinical testing
Natera, Inc. RCV001278205 SCV001465201 uncertain significance Usher syndrome type 1F 2020-08-13 no assertion criteria provided clinical testing

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