ClinVar Miner

Submissions for variant NM_017541.4(CRYGS):c.306G>A (p.Gly102=)

gnomAD frequency: 0.00176  dbSNP: rs114186269
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Total submissions: 3
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
GeneDx RCV001575295 SCV001802257 likely benign not provided 2020-11-30 criteria provided, single submitter clinical testing
Labcorp Genetics (formerly Invitae), Labcorp RCV002072257 SCV002474438 benign Cataract 20 multiple types 2024-01-22 criteria provided, single submitter clinical testing
Breakthrough Genomics, Breakthrough Genomics RCV001575295 SCV005263020 likely benign not provided criteria provided, single submitter not provided

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