ClinVar Miner

Submissions for variant NM_001164277.2(SLC37A4):c.831C>T (p.Ser277=)

gnomAD frequency: 0.00001  dbSNP: rs996156142
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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 RCV000928005 SCV001073606 likely benign Glucose-6-phosphate transport defect 2023-04-19 criteria provided, single submitter clinical testing

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