ClinVar Miner

Submissions for variant NM_000048.4(ASL):c.552T>C (p.Ser184=)

gnomAD frequency: 0.00001  dbSNP: rs1786675333
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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 RCV001489054 SCV001693588 likely benign Argininosuccinate lyase deficiency 2019-10-02 criteria provided, single submitter clinical testing

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