ClinVar Miner

Submissions for variant NM_018965.3(TREM2):c.469C>T (p.His157Tyr) (rs2234255)

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Total submissions: 4
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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 RCV000513757 SCV000609551 likely benign not provided 2017-06-16 criteria provided, single submitter clinical testing
EGL Genetic Diagnostics,Eurofins Clinical Diagnostics RCV000177312 SCV000229159 benign not specified 2015-05-11 criteria provided, single submitter clinical testing
Illumina Clinical Services Laboratory,Illumina RCV000352563 SCV000462947 likely benign Polycystic lipomembranous osteodysplasia with sclerosing leukoencephalopathy 2016-06-14 criteria provided, single submitter clinical testing
PreventionGenetics RCV000177312 SCV000313283 benign not specified criteria provided, single submitter clinical testing

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