ClinVar Miner

Submissions for variant NM_002473.5(MYH9):c.*8C>T (rs201455315)

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Total submissions: 3
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Laboratory for Molecular Medicine,Partners HealthCare Personalized Medicine RCV000215226 SCV000272063 uncertain significance not specified 2016-06-30 criteria provided, single submitter clinical testing Variant classified as Uncertain Significance - Favor Benign.
Illumina Clinical Services Laboratory,Illumina RCV000310238 SCV000438292 likely benign MYH9-related disorder 2016-06-14 criteria provided, single submitter clinical testing
Illumina Clinical Services Laboratory,Illumina RCV000367215 SCV000438293 likely benign Nonsyndromic Hearing Loss, Dominant 2016-06-14 criteria provided, single submitter clinical testing

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