Variant Gene Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs6983267
rs6983267
0.100 GeneticVariation BEFREE Associations among dietary seaweed intake, c-MYC rs6983267 polymorphism, and risk of colorectal cancer in a Korean population: a case-control study. 31300834

2019

dbSNP: rs6983267
rs6983267
0.100 GeneticVariation BEFREE In particular, both homozygous TT and heterozygous CT genotypes of rs10505477, as well as the GG and TG genotypes of rs6983267, were associated with risk of colorectal cancer.Our study provides summary evidence that common variants in the 8q24 are associated with risk of colorectal cancer in this large-scale research synopsis and meta-analysis. 30170403

2018

dbSNP: rs6983267
rs6983267
0.100 GeneticVariation BEFREE A polymorphic MYC response element in KBTBD11 influences colorectal cancer risk, especially in interaction with an MYC-regulated SNP rs6983267. 29267898

2018

dbSNP: rs6983267
rs6983267
0.100 GeneticVariation BEFREE Stratified analyses indicated that rs6983267 significantly increased the risk of colorectal cancer in Caucasians, prostate cancer in Caucasians and Asians, thyroid cancer in Caucasians and lung cancer in Asians. 28915683

2017

dbSNP: rs6983267
rs6983267
0.100 GeneticVariation BEFREE Association of rs6983267 at 8q24, HULC rs7763881 polymorphisms and serum lncRNAs CCAT2 and HULC with colorectal cancer in Egyptian patients. 29176650

2017

dbSNP: rs6983267
rs6983267
0.100 GeneticVariation BEFREE Association of 8q24.21 rs10505477-rs6983267 haplotype and age at diagnosis of colorectal cancer. 24528058

2014

dbSNP: rs6983267
rs6983267
0.100 GeneticVariation BEFREE Here, we report that CCAT2, a novel long noncoding RNA transcript (lncRNA) encompassing the rs6983267 SNP, is highly overexpressed in microsatellite-stable colorectal cancer and promotes tumor growth, metastasis, and chromosomal instability. 23796952

2013

dbSNP: rs6983267
rs6983267
0.100 GeneticVariation BEFREE The rs6983267 SNP is associated with MYC transcription efficiency, which promotes progression and worsens prognosis of colorectal cancer. 22976378

2013

dbSNP: rs6983267
rs6983267
0.100 GeneticVariation BEFREE Aspirin use, 8q24 single nucleotide polymorphism rs6983267, and colorectal cancer according to CTNNB1 alterations. 24317174

2013

dbSNP: rs6983267
rs6983267
0.100 GeneticVariation BEFREE A significant relation was found between rs6983267 variant in the 8q24 region and colorectal cancer. 21567271

2012

dbSNP: rs6983267
rs6983267
0.100 GeneticVariation BEFREE We found no significant differences between the association of rs6983267 and colorectal cancer and colorectal adenomas. 21455501

2011

dbSNP: rs6983267
rs6983267
0.100 GeneticVariation BEFREE The 8q24 cancer risk variant rs6983267 shows long-range interaction with MYC in colorectal cancer. 19561607

2009

dbSNP: rs6983267
rs6983267
0.100 GeneticVariation BEFREE The common colorectal cancer predisposition SNP rs6983267 at chromosome 8q24 confers potential to enhanced Wnt signaling. 19561604

2009

dbSNP: rs6983267
rs6983267
0.100 GeneticVariation BEFREE The rs6983267 locus is also strongly associated with colorectal cancer. 18704501

2008

dbSNP: rs6983267
rs6983267
0.100 GeneticVariation BEFREE We studied 1,807 affected individuals and 5,511 controls and found that one variant, rs6983267, is also significantly associated with colorectal cancer (odds ratio = 1.22; P = 4.4 x 10(-6)) and that the apportionment of risk among the variants differs significantly between the two cancers. 17618282

2007