ClinVar Miner

Submissions for variant NM_001048174.2(MUTYH):c.1102+42_1102+43del

gnomAD frequency: 0.00001  dbSNP: rs775033999
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Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Mendelics RCV000986301 SCV001135251 likely benign Familial adenomatous polyposis 2 2019-05-28 criteria provided, single submitter clinical testing
Center for Genomic Medicine, Rigshospitalet, Copenhagen University Hospital RCV002268384 SCV002552474 likely benign not specified 2025-03-04 criteria provided, single submitter clinical testing

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