ClinVar Miner

Submissions for variant NM_019109.4(ALG1):c.208+16_208+19dup (rs35400794)

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Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
EGL Genetic Diagnostics,Eurofins Clinical Diagnostics RCV000081985 SCV000113920 benign not specified 2014-05-06 criteria provided, single submitter clinical testing
Mendelics RCV000989515 SCV001139930 benign Congenital disorder of glycosylation type 1K 2019-05-28 criteria provided, single submitter clinical testing

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