ClinVar Miner

Submissions for variant NM_001164277.2(SLC37A4):c.366G>A (p.Gly122=)

dbSNP: rs1555191518
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Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Counsyl RCV000670914 SCV000795830 likely benign Glucose-6-phosphate transport defect 2017-11-19 criteria provided, single submitter clinical testing
Labcorp Genetics (formerly Invitae), Labcorp RCV000670914 SCV002356419 likely benign Glucose-6-phosphate transport defect 2021-05-24 criteria provided, single submitter clinical testing

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