ClinVar Miner

Submissions for variant NM_001164277.2(SLC37A4):c.537C>T (p.Val179=)

dbSNP: rs1780828602
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Total submissions: 1
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Labcorp Genetics (formerly Invitae), Labcorp RCV001469849 SCV001673938 likely benign Glucose-6-phosphate transport defect 2024-11-14 criteria provided, single submitter clinical testing

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