ClinVar Miner

Submissions for variant NM_133642.5(LARGE1):c.1452-28C>T

dbSNP: rs76647066
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Total submissions: 4
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Eurofins Ntd Llc (ga) RCV000081171 SCV000113079 benign not specified 2012-11-15 criteria provided, single submitter clinical testing
PreventionGenetics, part of Exact Sciences RCV000081171 SCV000310630 likely benign not specified criteria provided, single submitter clinical testing
GeneDx RCV001596952 SCV001831488 benign not provided 2018-07-15 criteria provided, single submitter clinical testing
Genetic Services Laboratory, University of Chicago RCV000081171 SCV000193503 likely benign not specified no assertion criteria provided clinical testing

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