ClinVar Miner

Submissions for variant NM_004562.3(PRKN):c.1180G>A (p.Asp394Asn) (rs1801334)

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Total submissions: 4
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
EGL Genetic Diagnostics,Eurofins Clinical Diagnostics RCV000244341 SCV000703282 benign not specified 2016-12-01 criteria provided, single submitter clinical testing
GeneReviews RCV000034121 SCV000058051 benign Parkinson disease 2 2001-04-17 no assertion criteria provided curation Converted during submission to Benign.
Invitae RCV000034121 SCV000560142 benign Parkinson disease 2 2017-07-27 criteria provided, single submitter clinical testing
PreventionGenetics RCV000244341 SCV000310474 benign not specified criteria provided, single submitter clinical testing

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