ClinVar Miner

Submissions for variant NM_002087.3(GRN):c.55C>T (p.Arg19Trp) (rs63750723)

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Total submissions: 7
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Ambry Genetics RCV000715766 SCV000846597 benign Seizures 2016-05-09 criteria provided, single submitter clinical testing
Athena Diagnostics Inc RCV000576325 SCV000677381 benign Frontotemporal dementia, ubiquitin-positive 2017-06-20 criteria provided, single submitter clinical testing
Center for Pediatric Genomic Medicine,Children's Mercy Hospital and Clinics RCV000084422 SCV000610102 benign not provided 2017-05-03 criteria provided, single submitter clinical testing
Illumina Clinical Services Laboratory,Illumina RCV000378525 SCV000403337 likely benign Frontotemporal dementia 2016-06-14 criteria provided, single submitter clinical testing
Invitae RCV000650264 SCV000772104 benign Frontotemporal dementia, ubiquitin-positive; Ceroid lipofuscinosis, neuronal, 11 2017-09-26 criteria provided, single submitter clinical testing
PreventionGenetics RCV000246460 SCV000308703 benign not specified criteria provided, single submitter clinical testing
VIB Department of Molecular Genetics, University of Antwerp RCV000084422 SCV000116558 not provided not provided no assertion provided not provided

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