ClinVar Miner

Submissions for variant NM_001278064.2(GRM1):c.1433+10T>C

gnomAD frequency: 0.00111  dbSNP: rs373538200
Minimum review status: Collection method:
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ClinVar version:
Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Athena Diagnostics Inc RCV001283512 SCV000613557 benign not specified 2020-04-17 criteria provided, single submitter clinical testing
Invitae RCV000517684 SCV001037322 likely benign not provided 2024-01-14 criteria provided, single submitter clinical testing

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