ClinVar Miner

Submissions for variant NM_019109.5(ALG1):c.630-19C>T

dbSNP: rs371014838
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Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Labcorp Genetics (formerly Invitae), Labcorp RCV002135814 SCV002453139 benign ALG1-congenital disorder of glycosylation 2024-01-18 criteria provided, single submitter clinical testing
Fulgent Genetics, Fulgent Genetics RCV002135814 SCV002794908 likely benign ALG1-congenital disorder of glycosylation 2021-08-18 criteria provided, single submitter clinical testing

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