ClinVar Miner

Submissions for variant NM_001142800.2(EYS):c.3164+7A>T

gnomAD frequency: 0.00004  dbSNP: rs963551759
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 RCV000977418 SCV001125335 likely benign not provided 2024-04-30 criteria provided, single submitter clinical testing
Women's Health and Genetics/Laboratory Corporation of America, LabCorp RCV003230609 SCV003929172 uncertain significance not specified 2023-04-17 criteria provided, single submitter clinical testing

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