ClinVar Miner

Submissions for variant NM_005359.6(SMAD4):c.*3878dup

dbSNP: rs373831598
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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 RCV000306921 SCV000409258 likely benign Juvenile Polyposis 2016-06-14 criteria provided, single submitter clinical testing
Illumina Laboratory Services, Illumina RCV000366283 SCV000409259 likely benign Telangiectasia, hereditary hemorrhagic, type 1 2016-06-14 criteria provided, single submitter clinical testing
Illumina Laboratory Services, Illumina RCV000400362 SCV000409260 likely benign Myhre syndrome 2016-06-14 criteria provided, single submitter clinical testing

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