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[Single-variant analysis identified a coding variant (rs3184504) in SH2B3 (12q24) associated with CRC risk (OR?=?1.08, P?=?3.9?�?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?�?10(-7)); rs6580742 and rs12303082 (12q13) in FAM186A (OR?=?1.11, P?=?1.2?�?10(-7) and OR?=?1.09, P?=?7.4?�?10(-8)); rs1129406 (12q13) in ATF1 (OR?=?1.11, P?=?8.3?�?10(-9)), all reaching exome-wide significance levels.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine.
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DisGeNET evidence - LITERATURE
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