ClinVar Miner

Submissions for variant NM_001142800.2(EYS):c.5928-35T>C

gnomAD frequency: 0.72606  dbSNP: rs587278
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Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Genome-Nilou Lab RCV001530499 SCV001745350 benign Retinitis pigmentosa 25 2021-07-01 criteria provided, single submitter clinical testing
GeneDx RCV001724345 SCV001950666 benign not provided 2015-03-03 criteria provided, single submitter clinical testing

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