ClinVar Miner

Submissions for variant NM_003896.4(ST3GAL5):c.129G>A (p.Ser43=)

dbSNP: rs776016166
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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 RCV001427305 SCV001629980 likely benign GM3 synthase deficiency 2023-11-19 criteria provided, single submitter clinical testing

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