ClinVar Miner

Submissions for variant NM_001164277.2(SLC37A4):c.626+7C>T

dbSNP: rs1555191207
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Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Counsyl RCV000666887 SCV000791256 likely benign Glucose-6-phosphate transport defect 2017-05-15 criteria provided, single submitter clinical testing
Labcorp Genetics (formerly Invitae), Labcorp RCV000666887 SCV001680822 likely benign Glucose-6-phosphate transport defect 2023-09-06 criteria provided, single submitter clinical testing

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