ClinVar Miner

Submissions for variant NM_001039891.3(ZNF674):c.707A>G (p.Lys236Arg) (rs201621696)

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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 RCV000079385 SCV000111264 benign not specified 2013-05-20 criteria provided, single submitter clinical testing
Illumina Clinical Services Laboratory,Illumina RCV000327307 SCV000482334 likely benign Non-syndromic X-linked intellectual disability 2016-06-14 criteria provided, single submitter clinical testing
Ambry Genetics RCV000720984 SCV000851868 uncertain significance History of neurodevelopmental disorder 2013-12-26 criteria provided, single submitter clinical testing Insufficient or inconclusive evidence

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