ClinVar Miner

Submissions for variant NM_001024845.3(SLC6A9):c.1536+11_1536+30del

dbSNP: rs549038505
Minimum review status: Collection method:
Minimum conflict level:
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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 RCV002115968 SCV002405377 benign Atypical glycine encephalopathy 2025-01-06 criteria provided, single submitter clinical testing

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