Variant Gene Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs6983267
rs6983267
0.760 GeneticVariation BEFREE In conclusion, some variants associated with CRC risk (rs10505477, rs6983267, rs10795668 and rs11255841) are also involved in the susceptibility to CRA and specific subtypes. 30194776

2019

dbSNP: rs6983267
rs6983267
G 0.760 GeneticVariation GWASCAT Discovery of common and rare genetic risk variants for colorectal cancer. 30510241

2019

dbSNP: rs6983267
rs6983267
0.760 GeneticVariation BEFREE This meta-analysis suggests that the 8q24.21-rs6983267 polymorphism is associated with CRC/CRA susceptibility, but these associations vary in different ethnic populations. 24375194

2014

dbSNP: rs6983267
rs6983267
0.760 GeneticVariation BEFREE Three polymorphic sites at chromosome 8q24 (rs7837328, rs10808555, rs6983267) have been associated with risk for colorectal adenomas. 23776012

2014

dbSNP: rs6983267
rs6983267
0.760 GeneticVariation BEFREE There was a statistically significant direct association of rs6983267 with colorectal adenoma that was consistent with those in previous reports. 24115145

2014

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

2011

dbSNP: rs6983267
rs6983267
0.760 GeneticVariation BEFREE The combination of rs6983267 on 8q24.21 and rs9929218 on 16q22.2 was associated with a history of colorectal adenoma (carriers of GG and AA, respectively; OR, 2.28; 95% CI, 1.32-3.93; P = 5.0 x 10(-4)). 20638935

2010

dbSNP: rs11255841
rs11255841
T 0.710 GeneticVariation GWASCAT Discovery of common and rare genetic risk variants for colorectal cancer. 30510241

2019

dbSNP: rs11255841
rs11255841
0.710 GeneticVariation BEFREE In conclusion, some variants associated with CRC risk (rs10505477, rs6983267, rs10795668 and rs11255841) are also involved in the susceptibility to CRA and specific subtypes. 30194776

2019

dbSNP: rs16892766
rs16892766
C 0.710 GeneticVariation GWASCAT Discovery of common and rare genetic risk variants for colorectal cancer. 30510241

2019

dbSNP: rs16892766
rs16892766
0.710 GeneticVariation BEFREE Our findings demonstrated that rs16892766-C allele might be risk-conferring factors for the development of CRC, but not for CRA. 25293934

2015

dbSNP: rs10049390
rs10049390
A 0.700 GeneticVariation GWASCAT Discovery of common and rare genetic risk variants for colorectal cancer. 30510241

2019

dbSNP: rs1078643
rs1078643
A 0.700 GeneticVariation GWASCAT Discovery of common and rare genetic risk variants for colorectal cancer. 30510241

2019

dbSNP: rs10821907
rs10821907
C 0.700 GeneticVariation GWASCAT Discovery of common and rare genetic risk variants for colorectal cancer. 30510241

2019

dbSNP: rs10849433
rs10849433
C 0.700 GeneticVariation GWASCAT Discovery of common and rare genetic risk variants for colorectal cancer. 30510241

2019

dbSNP: rs10980628
rs10980628
C 0.700 GeneticVariation GWASCAT Discovery of common and rare genetic risk variants for colorectal cancer. 30510241

2019

dbSNP: rs11087784
rs11087784
G 0.700 GeneticVariation GWASCAT Discovery of common and rare genetic risk variants for colorectal cancer. 30510241

2019

dbSNP: rs11190164
rs11190164
G 0.700 GeneticVariation GWASCAT Discovery of common and rare genetic risk variants for colorectal cancer. 30510241

2019

dbSNP: rs11196170
rs11196170
A 0.700 GeneticVariation GWASCAT Discovery of common and rare genetic risk variants for colorectal cancer. 30510241

2019

dbSNP: rs11610543
rs11610543
G 0.700 GeneticVariation GWASCAT Discovery of common and rare genetic risk variants for colorectal cancer. 30510241

2019

dbSNP: rs116353863
rs116353863
C 0.700 GeneticVariation GWASCAT Discovery of common and rare genetic risk variants for colorectal cancer. 30510241

2019

dbSNP: rs117079142
rs117079142
A 0.700 GeneticVariation GWASCAT Discovery of common and rare genetic risk variants for colorectal cancer. 30510241

2019

dbSNP: rs11727676
rs11727676
C 0.700 GeneticVariation GWASCAT Discovery of common and rare genetic risk variants for colorectal cancer. 30510241

2019

dbSNP: rs11874392
rs11874392
A 0.700 GeneticVariation GWASCAT Discovery of common and rare genetic risk variants for colorectal cancer. 30510241

2019

dbSNP: rs11884596
rs11884596
C 0.700 GeneticVariation GWASCAT Discovery of common and rare genetic risk variants for colorectal cancer. 30510241

2019