ClinVar Miner

Submissions for variant NM_001164277.2(SLC37A4):c.471C>T (p.Thr157=)

dbSNP: rs775227522
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Total submissions: 1
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Counsyl RCV000672476 SCV000797583 likely benign Glucose-6-phosphate transport defect 2018-01-31 criteria provided, single submitter clinical testing

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