ClinVar Miner

Submissions for variant NM_004895.4(NLRP3):c.*351dup

dbSNP: rs397821684
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Total submissions: 3
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Illumina Laboratory Services, Illumina RCV000396126 SCV000357022 benign Familial amyloid nephropathy with urticaria AND deafness 2016-06-14 criteria provided, single submitter clinical testing
Illumina Laboratory Services, Illumina RCV000310921 SCV000357023 benign Chronic infantile neurological, cutaneous and articular syndrome 2016-06-14 criteria provided, single submitter clinical testing
Illumina Laboratory Services, Illumina RCV000365636 SCV000357024 benign Familial cold autoinflammatory syndrome 2016-06-14 criteria provided, single submitter clinical testing

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