ClinVar Miner

Submissions for variant NM_000435.3(NOTCH3):c.1140T>C (p.Pro380=) (rs61749020)

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Total submissions: 3
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
PreventionGenetics,PreventionGenetics RCV000252960 SCV000304239 benign not specified criteria provided, single submitter clinical testing
Illumina Clinical Services Laboratory,Illumina RCV000362891 SCV000411008 likely benign Cerebral autosomal dominant arteriopathy with subcortical infarcts and leukoencephalopathy 2016-06-14 criteria provided, single submitter clinical testing
Athena Diagnostics Inc RCV000362891 SCV000677220 benign Cerebral autosomal dominant arteriopathy with subcortical infarcts and leukoencephalopathy 2017-05-31 criteria provided, single submitter clinical testing

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