ClinVar Miner

Submissions for variant NM_001024845.3(SLC6A9):c.645G>A (p.Leu215=)

dbSNP: rs200958790
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Total submissions: 1
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Labcorp Genetics (formerly Invitae), Labcorp RCV002177227 SCV002349147 likely benign Atypical glycine encephalopathy 2022-09-13 criteria provided, single submitter clinical testing

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