ClinVar Miner

Submissions for variant NM_001142800.2(EYS):c.5601T>C (p.Ser1867=) (rs182322608)

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Total submissions: 3
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
EGL Genetic Diagnostics,Eurofins Clinical Diagnostics RCV000079542 SCV000111424 benign not specified 2013-09-25 criteria provided, single submitter clinical testing
CeGaT Praxis fuer Humangenetik Tuebingen RCV000513065 SCV000609214 uncertain significance not provided 2017-03-31 criteria provided, single submitter clinical testing
Counsyl RCV000664906 SCV000788936 likely benign Retinitis pigmentosa 25 2017-03-06 criteria provided, single submitter clinical testing

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