ClinVar Miner

Submissions for variant NM_001142800.2(EYS):c.3633C>G (p.Leu1211=)

gnomAD frequency: 0.00001  dbSNP: rs765825077
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 RCV001422247 SCV001624790 likely benign not provided 2023-07-09 criteria provided, single submitter clinical testing

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