ClinVar Miner

Submissions for variant NM_003896.4(ST3GAL5):c.183C>T (p.Ser61=)

dbSNP: rs2104079146
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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 RCV001484042 SCV001688450 likely benign GM3 synthase deficiency 2022-02-04 criteria provided, single submitter clinical testing

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