ClinVar Miner

Submissions for variant NM_000048.4(ASL):c.656-3dup

dbSNP: rs778811159
Minimum review status: Collection method:
Minimum conflict level:
ClinVar version:
Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Labcorp Genetics (formerly Invitae), Labcorp RCV001519305 SCV001728150 benign Argininosuccinate lyase deficiency 2024-02-07 criteria provided, single submitter clinical testing
Fulgent Genetics, Fulgent Genetics RCV001519305 SCV002807887 likely benign Argininosuccinate lyase deficiency 2022-02-28 criteria provided, single submitter clinical testing

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