ClinVar Miner

Submissions for variant NM_001029883.3(PCARE):c.3669-2AGC[4]

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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 RCV000382560 SCV000341214 benign not specified 2016-04-14 criteria provided, single submitter clinical testing
Illumina Clinical Services Laboratory,Illumina RCV000278051 SCV000429853 likely benign Retinitis Pigmentosa, Recessive 2016-06-14 criteria provided, single submitter clinical testing
Mendelics RCV000986607 SCV001135644 benign Retinitis pigmentosa 54 2019-05-28 criteria provided, single submitter clinical testing
Invitae RCV001511102 SCV001718290 benign not provided 2020-11-26 criteria provided, single submitter clinical testing

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