ClinVar Miner

Submissions for variant NM_005208.5(CRYBA1):c.97-20G>A

gnomAD frequency: 0.00004  dbSNP: rs201548192
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Total submissions: 1
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Labcorp Genetics (formerly Invitae), Labcorp RCV002122640 SCV002408203 benign Cataract 10 multiple types 2023-10-13 criteria provided, single submitter clinical testing

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