ClinVar Miner

Submissions for variant NM_054012.4(ASS1):c.421-8A>T

dbSNP: rs764424984
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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 RCV001452242 SCV001655899 likely benign Citrullinemia 2023-08-19 criteria provided, single submitter clinical testing

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