ClinVar Miner

Submissions for variant NM_001164277.2(SLC37A4):c.417C>T (p.Ala139=)

dbSNP: rs2134638267
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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 RCV002217554 SCV002365855 likely benign Glucose-6-phosphate transport defect 2021-07-12 criteria provided, single submitter clinical testing

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