ClinVar Miner

Submissions for variant NM_001278064.2(GRM1):c.950+8TC[17]

dbSNP: rs72225459
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Total submissions: 3
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
GeneDx RCV001679825 SCV001898566 benign not provided 2021-05-12 criteria provided, single submitter clinical testing
Genome Diagnostics Laboratory, University Medical Center Utrecht RCV001796691 SCV002034281 benign not specified no assertion criteria provided clinical testing
Laboratory of Diagnostic Genome Analysis, Leiden University Medical Center (LUMC) RCV001679825 SCV002036560 likely benign not provided no assertion criteria provided clinical testing

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