Source: CURATED

Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs10795668
rs10795668
LOC105376400
CUI: C0009402
Disease: Colorectal Carcinoma
Colorectal Carcinoma 		G 0.900 GeneticVariation GWASCAT Large-Scale Genome-Wide Association Study of East Asians Identifies Loci Associated With Risk for Colorectal Cancer. 30529582

2019
dbSNP: rs10795668
rs10795668
LOC105376400
CUI: C0009402
Disease: Colorectal Carcinoma
Colorectal Carcinoma 		G 0.900 GeneticVariation GWASCAT Identification of Susceptibility Loci and Genes for Colorectal Cancer Risk. 26965516

2016
dbSNP: rs10795668
rs10795668
LOC105376400
CUI: C0009402
Disease: Colorectal Carcinoma
Colorectal Carcinoma 		G 0.900 GeneticVariation GWASCAT Large-scale genetic study in East Asians identifies six new loci associated with colorectal cancer risk. 24836286

2014
dbSNP: rs10795668
rs10795668
LOC105376400
CUI: C0009402
Disease: Colorectal Carcinoma
Colorectal Carcinoma 		G 0.900 GeneticVariation GWASDB Large-scale genetic study in East Asians identifies six new loci associated with colorectal cancer risk. 24836286

2014
dbSNP: rs10795668
rs10795668
LOC105376400
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
dbSNP: rs10795668
rs10795668
LOC105376400
CUI: C0009402
Disease: Colorectal Carcinoma
Colorectal Carcinoma 		A 0.900 GeneticVariation GWASDB 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