ClinVar Miner

Submissions for variant NM_001164277.2(SLC37A4):c.332G>A (p.Gly111Asp)

dbSNP: rs1356550790
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Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Counsyl RCV000665513 SCV000789651 uncertain significance Glucose-6-phosphate transport defect 2017-02-08 criteria provided, single submitter clinical testing
Labcorp Genetics (formerly Invitae), Labcorp RCV000665513 SCV001223795 uncertain significance Glucose-6-phosphate transport defect 2021-09-01 criteria provided, single submitter clinical testing

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