ClinVar Miner

Submissions for variant NM_001142800.2(EYS):c.2846+174T>G

gnomAD frequency: 0.01911  dbSNP: rs142709378
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
GeneDx RCV001779559 SCV002015223 likely benign not provided 2021-05-12 criteria provided, single submitter clinical testing
Breakthrough Genomics, Breakthrough Genomics RCV001779559 SCV005222144 likely benign not provided criteria provided, single submitter not provided

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