ClinVar Miner

Submissions for variant NM_000038.6(APC):c.4638_4639del (p.Asn1546fs)

dbSNP: rs1561594148
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Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
ARUP Laboratories, Molecular Genetics and Genomics, ARUP Laboratories RCV000757002 SCV000885023 pathogenic not provided 2017-07-14 criteria provided, single submitter clinical testing
Fulgent Genetics, Fulgent Genetics RCV002507327 SCV002800088 likely pathogenic Desmoid disease, hereditary; Familial adenomatous polyposis 1; Hepatocellular carcinoma; Gastric cancer; Colorectal cancer; Gastric adenocarcinoma and proximal polyposis of the stomach 2021-11-11 criteria provided, single submitter clinical testing

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