Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs16892766
rs16892766
CUI: C0009402
Disease: Colorectal Carcinoma
Colorectal Carcinoma
C 0.900 GeneticVariation GWASCAT Association analyses identify 31 new risk loci for colorectal cancer susceptibility. 31089142

2019

dbSNP: rs16892766
rs16892766
CUI: C0009402
Disease: Colorectal Carcinoma
Colorectal Carcinoma
C 0.900 GeneticVariation GWASCAT Novel Common Genetic Susceptibility Loci for Colorectal Cancer. 29917119

2019

dbSNP: rs16892766
rs16892766
CUI: C0009402
Disease: Colorectal Carcinoma
Colorectal Carcinoma
C 0.900 GeneticVariation GWASCAT Discovery of common and rare genetic risk variants for colorectal cancer. 30510241

2019

dbSNP: rs16892766
rs16892766
CUI: C0009402
Disease: Colorectal Carcinoma
Colorectal Carcinoma
C 0.900 GeneticVariation GWASCAT Genome-wide association study of colorectal cancer identifies six new susceptibility loci. 26151821

2015

dbSNP: rs16892766
rs16892766
CUI: C0009402
Disease: Colorectal Carcinoma
Colorectal Carcinoma
0.900 GeneticVariation GWASCAT Meta-analysis of new genome-wide association studies of colorectal cancer risk. 21761138

2012

dbSNP: rs16892766
rs16892766
CUI: C0009402
Disease: Colorectal Carcinoma
Colorectal Carcinoma
A 0.900 GeneticVariation GWASCAT In addition to the previously reported 8q24, 15q13 and 18q21 CRC risk loci, we identified two previously unreported associations: rs10795668, located at 10p14 (P = 2.5 x 10(-13) overall; P = 6.9 x 10(-12) replication), and rs16892766, at 8q23.3 (P = 3.3 x 10(-18) overall; P = 9.6 x 10(-17) replication), which tags a plausible causative gene, EIF3H. 18372905

2008