ClinVar Miner

Submissions for variant NM_001164277.2(SLC37A4):c.626+10C>A

dbSNP: rs757924969
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Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Counsyl RCV000669387 SCV000794135 likely benign Glucose-6-phosphate transport defect 2017-09-15 criteria provided, single submitter clinical testing
Labcorp Genetics (formerly Invitae), Labcorp RCV000669387 SCV001684214 likely benign Glucose-6-phosphate transport defect 2023-08-07 criteria provided, single submitter clinical testing

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