ClinVar Miner

Submissions for variant NM_000843.4(GRM6):c.336C>T (p.Phe112=)

dbSNP: rs62638200
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 RCV000086054 SCV002971054 likely benign not provided 2023-09-25 criteria provided, single submitter clinical testing
Retina International RCV000086054 SCV000118198 not provided not provided no assertion provided not provided

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