ClinVar Miner

Submissions for variant NM_017541.4(CRYGS):c.294C>A (p.Ile98=)

gnomAD frequency: 0.00198  dbSNP: rs140421841
Minimum review status: Collection method:
Minimum conflict level:
ClinVar version:
Total submissions: 1
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Labcorp Genetics (formerly Invitae), Labcorp RCV001521919 SCV001731340 benign Cataract 20 multiple types 2023-12-07 criteria provided, single submitter clinical testing

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