ClinVar Miner

Submissions for variant NM_001024845.3(SLC6A9):c.31-6225G>T

dbSNP: rs201727215
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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 RCV002192199 SCV002350166 likely benign Atypical glycine encephalopathy 2022-02-03 criteria provided, single submitter clinical testing

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