ClinVar Miner

Submissions for variant NM_017929.6(PEX26):c.911G>A (p.Arg304His) (rs17851387)

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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 RCV000374196 SCV000340762 likely benign not specified 2017-01-09 criteria provided, single submitter clinical testing
Invitae RCV000650266 SCV000772106 likely benign not provided 2018-08-02 criteria provided, single submitter clinical testing

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