ClinVar Miner

Submissions for variant NM_000844.4(GRM7):c.1750C>T (p.Leu584=)

gnomAD frequency: 0.01399  dbSNP: rs80099685
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
Labcorp Genetics (formerly Invitae), Labcorp RCV000966846 SCV001114202 benign not provided 2025-01-27 criteria provided, single submitter clinical testing
Breakthrough Genomics, Breakthrough Genomics RCV000966846 SCV005245663 benign not provided criteria provided, single submitter not provided

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