ClinVar Miner

Submissions for variant NM_000244.3(MEN1):c.1636= (p.Ala546=) (rs2959656)

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Total submissions: 3
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
EGL Genetic Diagnostics,Eurofins Clinical Diagnostics RCV000121334 SCV000203003 benign not specified 2018-06-22 criteria provided, single submitter clinical testing
ITMI RCV000121334 SCV000085508 not provided not specified 2013-09-19 no assertion provided reference population
Laboratory for Molecular Medicine,Partners HealthCare Personalized Medicine RCV000121334 SCV000539614 benign not specified 2016-03-29 criteria provided, single submitter clinical testing Variant identified in a genome or exome case(s) and assessed due to predicted null impact of the variant or pathogenic assertions in the literature or databases. Disclaimer: This variant has not undergone full assessment. The following are preliminary notes: Frequency

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