ClinVar Miner

Submissions for variant NM_000180.3(GUCY2D):c.3225-7C>T (rs79887212)

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Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
EGL Genetic Diagnostics,Eurofins Clinical Diagnostics RCV000175391 SCV000226865 benign not specified 2014-09-03 criteria provided, single submitter clinical testing
Invitae RCV000549770 SCV000649521 benign Cone-rod dystrophy 6; Leber congenital amaurosis 1 2017-05-07 criteria provided, single submitter clinical testing

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