ClinVar Miner

Submissions for variant NM_015247.2(CYLD):c.*4561G>A (rs17314948)

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Total submissions: 3
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Illumina Clinical Services Laboratory,Illumina RCV000401157 SCV000397558 benign Cylindromatosis, familial 2016-06-14 criteria provided, single submitter clinical testing
Illumina Clinical Services Laboratory,Illumina RCV000289482 SCV000397559 benign Trichoepithelioma multiple familial 2 2016-06-14 criteria provided, single submitter clinical testing
Illumina Clinical Services Laboratory,Illumina RCV000346744 SCV000397560 benign Spiegler-Brooke syndrome 2016-06-14 criteria provided, single submitter clinical testing

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