ClinVar Miner

Submissions for variant NM_001164277.2(SLC37A4):c.891G>A (p.Gly297=)

dbSNP: rs1388277495
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Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Counsyl RCV000671296 SCV000796257 likely benign Glucose-6-phosphate transport defect 2017-12-08 criteria provided, single submitter clinical testing
Labcorp Genetics (formerly Invitae), Labcorp RCV000671296 SCV001605807 likely benign Glucose-6-phosphate transport defect 2022-09-19 criteria provided, single submitter clinical testing

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