ClinVar Miner

Submissions for variant NM_003073.5(SMARCB1):c.*116dup

dbSNP: rs397897183
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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 RCV000365731 SCV000437540 benign Schwannomatosis 2016-06-14 criteria provided, single submitter clinical testing
Illumina Laboratory Services, Illumina RCV000402538 SCV000437541 benign Rhabdoid tumor predisposition syndrome 2016-06-14 criteria provided, single submitter clinical testing
GeneDx RCV001712131 SCV001945663 benign not provided 2018-06-23 criteria provided, single submitter clinical testing

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