ClinVar Miner

Submissions for variant NM_019109.5(ALG1):c.863-84G>A

gnomAD frequency: 0.50001  dbSNP: rs1846690
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Total submissions: 3
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Genome-Nilou Lab RCV001549008 SCV001769047 benign ALG1-congenital disorder of glycosylation 2021-07-14 criteria provided, single submitter clinical testing
GeneDx RCV001615296 SCV001839455 benign not provided 2018-06-29 criteria provided, single submitter clinical testing
Breakthrough Genomics, Breakthrough Genomics RCV001615296 SCV005296520 benign not provided criteria provided, single submitter not provided

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