. . . . . . . "[Single-variant analysis identified a coding variant (rs3184504) in SH2B3 (12q24) associated with CRC risk (OR?=?1.08, P?=?3.9?\uFFFD?10(-7)), and novel damaging coding variants in 3 genes previously tagged by GWAS efforts; rs16888728 (8q24) in UTP23 (OR?=?1.15, P?=?1.4?\uFFFD?10(-7)); rs6580742 and rs12303082 (12q13) in FAM186A (OR?=?1.11, P?=?1.2?\uFFFD?10(-7) and OR?=?1.09, P?=?7.4?\uFFFD?10(-8)); rs1129406 (12q13) in ATF1 (OR?=?1.11, P?=?8.3?\uFFFD?10(-9)), all reaching exome-wide significance levels.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine."@en . . . . . "2017-02-19"^^ . . "Gene-disease associations inferred from text-mining the literature."@en . "DisGeNET evidence - LITERATURE"@en . "2017-10-17T13:10:45+02:00"^^ . . . . . . . . . . . "v5.0.0.0" . "v5.0.0" .