ClinVar Miner

Submissions for variant NM_000843.4(GRM6):c.504+20G>C

gnomAD frequency: 0.00374  dbSNP: rs572890701
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Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Eurofins Ntd Llc (ga) RCV000357235 SCV000341663 uncertain significance not provided 2016-05-25 criteria provided, single submitter clinical testing
Labcorp Genetics (formerly Invitae), Labcorp RCV000357235 SCV001716585 benign not provided 2024-01-24 criteria provided, single submitter clinical testing

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