ClinVar Miner

Submissions for variant NM_000843.4(GRM6):c.1221G>A (p.Ala407=)

gnomAD frequency: 0.00001  dbSNP: rs544297690
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 RCV001959650 SCV002248432 likely benign not provided 2024-09-15 criteria provided, single submitter clinical testing
Breakthrough Genomics, Breakthrough Genomics RCV001959650 SCV005188756 uncertain significance not provided criteria provided, single submitter not provided

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