ClinVar Miner

Submissions for variant NM_000435.3(NOTCH3):c.6753C>T (p.Ser2251=) (rs61731975)

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Total submissions: 4
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
PreventionGenetics,PreventionGenetics RCV000252208 SCV000304276 benign not specified criteria provided, single submitter clinical testing
Illumina Clinical Services Laboratory,Illumina RCV000375719 SCV000410937 benign Cerebral autosomal dominant arteriopathy with subcortical infarcts and leukoencephalopathy 2016-06-14 criteria provided, single submitter clinical testing
Athena Diagnostics Inc RCV000252208 SCV000614329 benign not specified 2017-05-02 criteria provided, single submitter clinical testing
Invitae RCV000870674 SCV001012199 benign not provided 2019-02-07 criteria provided, single submitter clinical testing

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