ClinVar Miner

Submissions for variant NM_017541.4(CRYGS):c.24T>A (p.Ile8=)

gnomAD frequency: 0.00359  dbSNP: rs113031838
Minimum review status: Collection method:
Minimum conflict level:
ClinVar version:
Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Labcorp Genetics (formerly Invitae), Labcorp RCV000637063 SCV000758511 benign Cataract 20 multiple types 2021-10-02 criteria provided, single submitter clinical testing
Breakthrough Genomics, Breakthrough Genomics RCV004717695 SCV005305180 benign not provided criteria provided, single submitter not provided

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