ClinVar Miner

Submissions for variant NM_000844.4(GRM7):c.144C>T (p.Asp48=)

gnomAD frequency: 0.00153  dbSNP: rs142650646
Minimum review status: Collection method:
Minimum conflict level:
Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
CeGaT Center for Human Genetics Tuebingen RCV000908103 SCV001746749 likely benign not provided 2024-06-01 criteria provided, single submitter clinical testing GRM7: BP4, BP7
Labcorp Genetics (formerly Invitae), Labcorp RCV000908103 SCV001052844 benign not provided 2026-01-19 criteria provided, single submitter clinical testing

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