ClinVar Miner

Submissions for variant NM_018965.3(TREM2):c.287C>A (p.Thr96Lys) (rs2234253)

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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 RCV000444438 SCV000511041 benign not provided 2016-09-12 criteria provided, single submitter clinical testing
EGL Genetic Diagnostics,Eurofins Clinical Diagnostics RCV000591330 SCV000703579 benign not specified 2016-11-22 criteria provided, single submitter clinical testing
Illumina Clinical Services Laboratory,Illumina RCV000312921 SCV000462949 likely benign Polycystic lipomembranous osteodysplasia with sclerosing leukoencephalopathy 2016-06-14 criteria provided, single submitter clinical testing

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