ClinVar Miner

Submissions for variant NM_201253.3(CRB1):c.479G>A (p.Gly160Glu)

dbSNP: rs1352663513
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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 RCV004690045 SCV005184514 uncertain significance not specified 2024-05-28 criteria provided, single submitter clinical testing
Natera, Inc. RCV001277518 SCV001464478 uncertain significance Leber congenital amaurosis 2020-08-14 no assertion criteria provided clinical testing

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