ClinVar Miner

Submissions for variant NM_000038.6(APC):c.622C>A (p.Gln208Lys)

dbSNP: rs137854583
Minimum review status: Collection method:
Minimum conflict level:
ClinVar version:
Total submissions: 1
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Pathway Genomics RCV000144572 SCV000189868 uncertain significance Familial adenomatous polyposis 1 2014-07-24 no assertion criteria provided clinical testing

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