ClinVar Miner

Submissions for variant NM_000038.6(APC):c.6150_6151del (p.Lys2052fs)

dbSNP: rs1561605508
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Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
PreventionGenetics, part of Exact Sciences RCV000679076 SCV000805448 likely pathogenic not provided 2017-12-20 criteria provided, single submitter clinical testing
Baylor Genetics RCV003459649 SCV004207294 likely pathogenic Familial adenomatous polyposis 1 2022-12-28 criteria provided, single submitter clinical testing

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