ClinVar Miner

Submissions for variant NM_018965.3(TREM2):c.185G>A (p.Arg62His) (rs143332484)

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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 RCV000513870 SCV000610218 likely benign not provided 2017-02-20 criteria provided, single submitter clinical testing
DNA and Cytogenetics Diagnostics Unit,Erasmus Medical Center RCV000625434 SCV000745350 benign Polycystic lipomembranous osteodysplasia with sclerosing leukoencephalopathy 2015-09-21 criteria provided, single submitter clinical testing
EGL Genetic Diagnostics,Eurofins Clinical Diagnostics RCV000591525 SCV000705438 benign not specified 2017-01-25 criteria provided, single submitter clinical testing
Genome Diagnostics Laboratory,VU University Medical Center Amsterdam RCV000625434 SCV000745889 likely benign Polycystic lipomembranous osteodysplasia with sclerosing leukoencephalopathy 2015-09-14 no assertion criteria provided clinical testing

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