ClinVar Miner

Submissions for variant NM_001048174.2(MUTYH):c.1145_1146dup (p.Pro383fs)

dbSNP: rs1553125914
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Total submissions: 1
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Division of Human Genetics, Children's Hospital of Philadelphia RCV000477814 SCV000536829 likely pathogenic Familial adenomatous polyposis 2; Neoplasm of stomach 2015-11-12 no assertion criteria provided research

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