ClinVar Miner

Submissions for variant NM_001278064.2(GRM1):c.2007G>T (p.Ala669=)

dbSNP: rs148926588
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Total submissions: 3
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Athena Diagnostics RCV000711855 SCV000842261 benign not provided 2019-04-27 criteria provided, single submitter clinical testing
Labcorp Genetics (formerly Invitae), Labcorp RCV000711855 SCV001041377 benign not provided 2024-01-23 criteria provided, single submitter clinical testing
Fulgent Genetics, Fulgent Genetics RCV002499287 SCV002804816 likely benign Autosomal recessive spinocerebellar ataxia 13; Spinocerebellar ataxia 44 2022-01-06 criteria provided, single submitter clinical testing

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