ClinVar Miner

Submissions for variant NM_014239.4(EIF2B2):c.*180G>C (rs4556)

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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 RCV000295805 SCV000388727 benign Leukoencephalopathy with vanishing white matter 2016-06-14 criteria provided, single submitter clinical testing
Illumina Clinical Services Laboratory,Illumina RCV000299748 SCV000483493 likely benign Lynch syndrome 2016-06-14 criteria provided, single submitter clinical testing

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