ClinVar Miner

Submissions for variant NM_001278064.2(GRM1):c.2922T>C (p.Pro974=)

gnomAD frequency: 0.00065  dbSNP: rs142409803
Minimum review status: Collection method:
Minimum conflict level:
ClinVar version:
Total submissions: 3
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Athena Diagnostics Inc RCV001644774 SCV000842268 benign not specified 2021-02-10 criteria provided, single submitter clinical testing
Invitae RCV000711862 SCV001039189 benign not provided 2024-01-24 criteria provided, single submitter clinical testing
CeGaT Center for Human Genetics Tuebingen RCV000711862 SCV001746875 likely benign not provided 2023-10-01 criteria provided, single submitter clinical testing GRM1: BP4, BP7

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