ClinVar Miner

Submissions for variant NM_001164277.2(SLC37A4):c.381+8C>T

dbSNP: rs782284449
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Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Counsyl RCV000668704 SCV000793348 likely benign Glucose-6-phosphate transport defect 2017-08-23 criteria provided, single submitter clinical testing
Labcorp Genetics (formerly Invitae), Labcorp RCV000668704 SCV001615422 likely benign Glucose-6-phosphate transport defect 2024-01-29 criteria provided, single submitter clinical testing

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