ClinVar Miner

Submissions for variant NM_005215.4(DCC):c.3872G>A (p.Arg1291Gln)

dbSNP: rs768577706
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Total submissions: 1
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
CSER _CC_NCGL, University of Washington RCV000417336 SCV000503562 uncertain significance Colorectal cancer 2016-08-01 no assertion criteria provided research This gene does not have an established association with colon cancer risk. Found in patient having exome sequencing due to suspicion for hereditary colon cancer and/or polyps. Patient is a 43 year old with 5-10 colon polyps and a family history of colon cancer.

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