ClinVar Miner

Submissions for variant NM_001164277.2(SLC37A4):c.786-18_786-16del

dbSNP: rs1555191005
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Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Counsyl RCV000669001 SCV000793695 likely benign Glucose-6-phosphate transport defect 2017-08-22 criteria provided, single submitter clinical testing
Labcorp Genetics (formerly Invitae), Labcorp RCV000669001 SCV004686275 likely benign Glucose-6-phosphate transport defect 2023-01-18 criteria provided, single submitter clinical testing

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