ClinVar Miner

Submissions for variant NM_001164277.2(SLC37A4):c.1101C>T (p.Ala367=)

dbSNP: rs1555190455
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Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Counsyl RCV000672798 SCV000797941 likely benign Glucose-6-phosphate transport defect 2018-02-15 criteria provided, single submitter clinical testing
Labcorp Genetics (formerly Invitae), Labcorp RCV000672798 SCV004539897 likely benign Glucose-6-phosphate transport defect 2023-06-23 criteria provided, single submitter clinical testing

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