ClinVar Miner

Submissions for variant NM_000843.4(GRM6):c.2420C>T (p.Ala807Val)

gnomAD frequency: 0.06684  dbSNP: rs17078874
Minimum review status: Collection method:
Minimum conflict level:
ClinVar version:
Total submissions: 4
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Invitae RCV000086049 SCV001723560 benign not provided 2024-01-31 criteria provided, single submitter clinical testing
GeneDx RCV000086049 SCV001846204 benign not provided 2015-03-03 criteria provided, single submitter clinical testing
Retina International RCV000086049 SCV000118193 not provided not provided no assertion provided not provided
NEI Ophthalmic Genomics Laboratory, National Institutes of Health RCV000086049 SCV000119187 not provided not provided no assertion provided not provided

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