ClinVar Miner

Submissions for variant NM_001278064.2(GRM1):c.1602+52G>A

gnomAD frequency: 0.01949  dbSNP: rs362892
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Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
GeneDx RCV001779701 SCV002015459 likely benign not provided 2021-05-13 criteria provided, single submitter clinical testing
Breakthrough Genomics, Breakthrough Genomics RCV001779701 SCV005227806 likely benign not provided criteria provided, single submitter not provided

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