ClinVar Miner

Submissions for variant NM_001164277.2(SLC37A4):c.872-15_872-9dup

dbSNP: rs782321213
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Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Counsyl RCV000668018 SCV000792560 uncertain significance Glucose-6-phosphate transport defect 2017-06-30 criteria provided, single submitter clinical testing
Labcorp Genetics (formerly Invitae), Labcorp RCV000668018 SCV002333780 likely benign Glucose-6-phosphate transport defect 2023-12-26 criteria provided, single submitter clinical testing

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