ClinVar Miner

Submissions for variant NM_004525.2(LRP2):c.13610A>C (p.Gln4537Pro) (rs188918037)

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Total submissions: 3
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Center for Pediatric Genomic Medicine,Children's Mercy Hospital and Clinics RCV000423936 SCV000511726 likely benign not provided 2016-12-30 criteria provided, single submitter clinical testing Converted during submission to Likely benign.
Genetic Services Laboratory, University of Chicago RCV000194145 SCV000247859 uncertain significance not specified 2014-08-14 criteria provided, single submitter clinical testing
Illumina Clinical Services Laboratory,Illumina RCV000374226 SCV000419012 likely benign Donnai Barrow syndrome 2016-06-14 criteria provided, single submitter clinical testing

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