ClinVar Miner

Submissions for variant NM_000843.4(GRM6):c.19G>A (p.Ala7Thr)

gnomAD frequency: 0.00533  dbSNP: rs62642053
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Total submissions: 7
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Eurofins Ntd Llc (ga) RCV000259068 SCV000111196 benign not specified 2016-11-04 criteria provided, single submitter clinical testing
CeGaT Center for Human Genetics Tuebingen RCV000079326 SCV000892535 likely benign not provided 2024-06-01 criteria provided, single submitter clinical testing GRM6: PP2, BS2
Labcorp Genetics (formerly Invitae), Labcorp RCV000079326 SCV001029340 benign not provided 2025-02-03 criteria provided, single submitter clinical testing
Breakthrough Genomics, Breakthrough Genomics RCV000079326 SCV005222620 likely benign not provided criteria provided, single submitter not provided
Retina International RCV000079326 SCV000118186 not provided not provided no assertion provided not provided
Clinical Genetics, Academic Medical Center RCV000259068 SCV001922446 benign not specified no assertion criteria provided clinical testing
Clinical Genetics DNA and cytogenetics Diagnostics Lab, Erasmus MC, Erasmus Medical Center RCV000079326 SCV001967073 likely benign not provided no assertion criteria provided clinical testing

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