ClinVar Miner

Submissions for variant NM_001278064.2(GRM1):c.3206C>T (p.Pro1069Leu)

gnomAD frequency: 0.00337  dbSNP: rs79336287
Minimum review status: Collection method:
Minimum conflict level:
ClinVar version:
Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Athena Diagnostics Inc RCV000516297 SCV000613564 benign not provided 2019-08-05 criteria provided, single submitter clinical testing
Invitae RCV000516297 SCV001029172 likely benign not provided 2023-12-12 criteria provided, single submitter clinical testing

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