ClinVar Miner

Submissions for variant NM_000048.4(ASL):c.13-8C>T

dbSNP: rs2115689858
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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 RCV001429341 SCV001632055 likely benign Argininosuccinate lyase deficiency 2023-12-18 criteria provided, single submitter clinical testing

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