ClinVar Miner

Submissions for variant NM_054012.4(ASS1):c.566+8C>T

dbSNP: rs773713440
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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 RCV001429671 SCV001632388 likely benign Citrullinemia 2022-09-13 criteria provided, single submitter clinical testing

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