ClinVar Miner

Submissions for variant NM_000843.4(GRM6):c.1695G>A (p.Thr565=)

gnomAD frequency: 0.00001  dbSNP: rs794727907
Minimum review status: Collection method:
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ClinVar version:
Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Eurofins Ntd Llc (ga) RCV000180190 SCV000232582 uncertain significance not provided 2015-04-28 criteria provided, single submitter clinical testing
Labcorp Genetics (formerly Invitae), Labcorp RCV000180190 SCV005800653 likely benign not provided 2024-08-07 criteria provided, single submitter clinical testing

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