ClinVar Miner

Submissions for variant NM_001164277.2(SLC37A4):c.148+16G>A

dbSNP: rs2134643318
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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 RCV002082062 SCV002423610 likely benign Glucose-6-phosphate transport defect 2021-11-22 criteria provided, single submitter clinical testing

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