ClinVar Miner

Submissions for variant NM_000844.4(GRM7):c.1789C>T (p.Leu597=)

gnomAD frequency: 0.22935  dbSNP: rs7614915
Minimum review status: Collection method:
Minimum conflict level:
Total submissions: 3
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Breakthrough Genomics, Breakthrough Genomics RCV001519692 SCV005245664 benign not provided criteria provided, single submitter not provided
GeneDx RCV001519692 SCV001987403 benign not provided 2021-10-26 criteria provided, single submitter clinical testing
Labcorp Genetics (formerly Invitae), Labcorp RCV001519692 SCV001728604 benign not provided 2026-02-03 criteria provided, single submitter clinical testing

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