ClinVar Miner

Submissions for variant NM_000038.6(APC):c.*210_*213del

dbSNP: rs763673039
Minimum review status: Collection method:
Minimum conflict level:
ClinVar version:
Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Illumina Laboratory Services, Illumina RCV000347753 SCV000452061 uncertain significance APC-Associated Polyposis Disorders 2016-06-14 criteria provided, single submitter clinical testing
CeGaT Center for Human Genetics Tuebingen RCV002512080 SCV002821310 likely benign not provided 2024-03-01 criteria provided, single submitter clinical testing APC: BS1

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