ClinVar Miner

Submissions for variant NM_001887.4(CRYBB1):c.299+16C>A

dbSNP: rs57400078
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Total submissions: 3
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
GeneDx RCV001696426 SCV001916078 benign not provided 2018-09-05 criteria provided, single submitter clinical testing
Labcorp Genetics (formerly Invitae), Labcorp RCV002073255 SCV002403192 benign Cataract 17 multiple types 2024-01-18 criteria provided, single submitter clinical testing
Breakthrough Genomics, Breakthrough Genomics RCV001696426 SCV005273838 benign not provided criteria provided, single submitter not provided

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