ClinVar Miner

Submissions for variant NM_003896.4(ST3GAL5):c.1179G>A (p.Thr393=)

gnomAD frequency: 0.00001  dbSNP: rs757685346
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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 RCV001350503 SCV001544907 likely benign GM3 synthase deficiency 2024-01-03 criteria provided, single submitter clinical testing

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