ClinVar Miner

Submissions for variant NM_001164277.2(SLC37A4):c.891G>T (p.Gly297=)

dbSNP: rs1388277495
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Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Labcorp Genetics (formerly Invitae), Labcorp RCV001241820 SCV001414869 likely benign Glucose-6-phosphate transport defect 2023-05-24 criteria provided, single submitter clinical testing
Natera, Inc. RCV001241820 SCV001466214 uncertain significance Glucose-6-phosphate transport defect 2020-04-16 no assertion criteria provided clinical testing

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