ClinVar Miner

Submissions for variant NM_001164277.2(SLC37A4):c.627-20C>T

dbSNP: rs1191557410
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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 RCV002195582 SCV002359726 likely benign Glucose-6-phosphate transport defect 2021-05-19 criteria provided, single submitter clinical testing

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