ClinVar Miner

Submissions for variant NM_000844.4(GRM7):c.2388G>A (p.Thr796=)

gnomAD frequency: 0.00020  dbSNP: rs117160055
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 RCV000971692 SCV001119351 benign not provided 2023-10-04 criteria provided, single submitter clinical testing
CeGaT Center for Human Genetics Tuebingen RCV000971692 SCV004184377 likely benign not provided 2023-11-01 criteria provided, single submitter clinical testing GRM7: BP4, BP7

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