ClinVar Miner

Submissions for variant NM_002633.3(PGM1):c.*231C>T (rs886046483)

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Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Illumina Clinical Services Laboratory,Illumina RCV000293488 SCV000358680 uncertain significance Congenital disorder of glycosylation type 1t 2016-06-14 criteria provided, single submitter clinical testing
Illumina Clinical Services Laboratory,Illumina RCV000348511 SCV000358681 uncertain significance Congenital disorder of glycosylation 2016-06-14 criteria provided, single submitter clinical testing

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