ClinVar Miner

Submissions for variant NM_001164277.2(SLC37A4):c.871+19C>T

dbSNP: rs782487764
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Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Counsyl RCV000669512 SCV000794270 likely benign Glucose-6-phosphate transport defect 2017-10-06 criteria provided, single submitter clinical testing
Labcorp Genetics (formerly Invitae), Labcorp RCV000669512 SCV003474760 likely benign Glucose-6-phosphate transport defect 2023-10-04 criteria provided, single submitter clinical testing

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