COLCA2, colorectal cancer associated 2, 120376

N. diseases: 12; N. variants: 3
Source: ALL
Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs3802842
rs3802842
Entrez Id: 120376;399948
Gene Symbol: COLCA2;COLCA1
COLCA2;COLCA1
CUI: C0009402
Disease:
Colorectal Carcinoma
0.900 GeneticVariation BEFREE We used meta-analysis of an efficient empirical-Bayes estimator to detect potential multiplicative interactions between each of the SNPs [rs16892766 at 8q23.3 (EIF3H/UTP23), rs6983267 at 8q24 (MYC), rs10795668 at 10p14 (FLJ3802842), rs3802842 at 11q23 (LOC120376), rs4444235 at 14q22.2 (BMP4), rs4779584 at 15q13 (GREM1), rs9929218 at 16q22.1 (CDH1), rs4939827 at 18q21 (SMAD7), rs10411210 at 19q13.1 (RHPN2), and rs961253 at 20p12.3 (BMP2)] and select major CRC risk factors (sex, body mass index, height, smoking status, aspirin/nonsteroidal anti-inflammatory drug use, alcohol use, and dietary intake of calcium, folate, red meat, processed meat, vegetables, fruit, and fiber). 22367214 2012
dbSNP: rs3802842
rs3802842
Entrez Id: 120376;399948
Gene Symbol: COLCA2;COLCA1
COLCA2;COLCA1
CUI: C0007102
Disease:
Malignant tumor of colon
0.720 GeneticVariation GWASCAT Meta-analysis of new genome-wide association studies of colorectal cancer risk. 21761138 2012
dbSNP: rs3802842
rs3802842
Entrez Id: 120376;399948
Gene Symbol: COLCA2;COLCA1
COLCA2;COLCA1
CUI: C1319315
Disease:
Adenocarcinoma of large intestine
0.700 GeneticVariation GWASCAT Meta-analysis of new genome-wide association studies of colorectal cancer risk. 21761138 2012
dbSNP: rs3802842
rs3802842
Entrez Id: 120376;399948
Gene Symbol: COLCA2;COLCA1
COLCA2;COLCA1
CUI: C0346629
Disease:
Malignant neoplasm of large intestine
0.700 GeneticVariation GWASCAT Meta-analysis of new genome-wide association studies of colorectal cancer risk. 21761138 2012
dbSNP: rs3802842
rs3802842
Entrez Id: 120376;399948
Gene Symbol: COLCA2;COLCA1
COLCA2;COLCA1
CUI: C2675481
Disease:
COLORECTAL CANCER, SUSCEPTIBILITY TO, 10
0.700 GeneticVariation GWASCAT Meta-analysis of new genome-wide association studies of colorectal cancer risk. 21761138 2012
dbSNP: rs3802842
rs3802842
Entrez Id: 120376;399948
Gene Symbol: COLCA2;COLCA1
COLCA2;COLCA1
CUI: C0009404
Disease:
Colorectal Neoplasms
0.700 GeneticVariation GWASCAT Meta-analysis of new genome-wide association studies of colorectal cancer risk. 21761138 2012
dbSNP: rs3802842
rs3802842
Entrez Id: 120376;399948
Gene Symbol: COLCA2;COLCA1
COLCA2;COLCA1
CUI: C3554460
Disease:
COLORECTAL CANCER, SUSCEPTIBILITY TO, 12
0.700 GeneticVariation GWASCAT Meta-analysis of new genome-wide association studies of colorectal cancer risk. 21761138 2012
dbSNP: rs3802842
rs3802842
Entrez Id: 120376;399948
Gene Symbol: COLCA2;COLCA1
COLCA2;COLCA1
CUI: C1837315
Disease:
COLORECTAL CANCER, SUSCEPTIBILITY TO, 1
0.700 GeneticVariation GWASCAT Meta-analysis of new genome-wide association studies of colorectal cancer risk. 21761138 2012
dbSNP: rs3802842
rs3802842
Entrez Id: 120376;399948
Gene Symbol: COLCA2;COLCA1
COLCA2;COLCA1
CUI: C2677123
Disease:
COLORECTAL CANCER, SUSCEPTIBILITY TO, 3
0.700 GeneticVariation GWASCAT Meta-analysis of new genome-wide association studies of colorectal cancer risk. 21761138 2012
dbSNP: rs3802842
rs3802842
Entrez Id: 120376;399948
Gene Symbol: COLCA2;COLCA1
COLCA2;COLCA1
CUI: C4552100
Disease:
Lynch Syndrome
0.030 GeneticVariation BEFREE Regarding early-onset cases, 14q22 (rs4444235), 11q23 (rs3802842) and 20p12 (rs961253) variants were more associated with family history of CRC or tumors of the Lynch syndrome spectrum excluding CRC. 22235025 2012
dbSNP: rs3802842
rs3802842
Entrez Id: 120376;399948
Gene Symbol: COLCA2;COLCA1
COLCA2;COLCA1
CUI: C1333990
Disease:
Hereditary Nonpolyposis Colorectal Cancer
0.030 GeneticVariation BEFREE Regarding early-onset cases, 14q22 (rs4444235), 11q23 (rs3802842) and 20p12 (rs961253) variants were more associated with family history of CRC or tumors of the Lynch syndrome spectrum excluding CRC. 22235025 2012
dbSNP: rs3802842
rs3802842
Entrez Id: 120376;399948
Gene Symbol: COLCA2;COLCA1
COLCA2;COLCA1
CUI: C0034885
Disease:
Rectal Neoplasms
0.010 GeneticVariation BEFREE Carrying the C allele at rs3802842 appeared to be associated with a lower risk for rectal tumors in our dataset. 22457859 2012
dbSNP: rs3802842
rs3802842
Entrez Id: 120376;399948
Gene Symbol: COLCA2;COLCA1
COLCA2;COLCA1
CUI: C0034882
Disease:
Rectal Diseases
0.010 GeneticVariation BEFREE Several loci showed statistically significant associations with specific phenotypes notably rs6691170 and rs3802842 associated with microsatellite stable rectal disease; rs4779584, rs961253 and rs4813802 associated with microsatellite stable colonic disease and rs4444235 and rs4925386 with microsatellite instability colonic disease. 22045029 2012
dbSNP: rs3802842
rs3802842
Entrez Id: 120376;399948
Gene Symbol: COLCA2;COLCA1
COLCA2;COLCA1
CUI: C0009373
Disease:
Colonic Diseases
0.010 GeneticVariation BEFREE Several loci showed statistically significant associations with specific phenotypes notably rs6691170 and rs3802842 associated with microsatellite stable rectal disease; rs4779584, rs961253 and rs4813802 associated with microsatellite stable colonic disease and rs4444235 and rs4925386 with microsatellite instability colonic disease. 22045029 2012
dbSNP: rs3802842
rs3802842
Entrez Id: 120376;399948
Gene Symbol: COLCA2;COLCA1
COLCA2;COLCA1
CUI: C0237123
Disease:
Alcohol or Other Drugs use
0.010 GeneticVariation BEFREE We used meta-analysis of an efficient empirical-Bayes estimator to detect potential multiplicative interactions between each of the SNPs [rs16892766 at 8q23.3 (EIF3H/UTP23), rs6983267 at 8q24 (MYC), rs10795668 at 10p14 (FLJ3802842), rs3802842 at 11q23 (LOC120376), rs4444235 at 14q22.2 (BMP4), rs4779584 at 15q13 (GREM1), rs9929218 at 16q22.1 (CDH1), rs4939827 at 18q21 (SMAD7), rs10411210 at 19q13.1 (RHPN2), and rs961253 at 20p12.3 (BMP2)] and select major CRC risk factors (sex, body mass index, height, smoking status, aspirin/nonsteroidal anti-inflammatory drug use, alcohol use, and dietary intake of calcium, folate, red meat, processed meat, vegetables, fruit, and fiber). 22367214 2012
dbSNP: rs3802842
rs3802842
Entrez Id: 120376;399948
Gene Symbol: COLCA2;COLCA1
COLCA2;COLCA1
CUI: C0009402
Disease:
Colorectal Carcinoma
0.900 GeneticVariation GWASCAT Identification of Genetic Susceptibility Loci for Colorectal Tumors in a Genome-Wide Meta-analysis. 23266556 2013
dbSNP: rs3802842
rs3802842
Entrez Id: 120376;399948
Gene Symbol: COLCA2;COLCA1
COLCA2;COLCA1
CUI: C0009402
Disease:
Colorectal Carcinoma
0.900 GeneticVariation GWASDB Identification of Genetic Susceptibility Loci for Colorectal Tumors in a Genome-Wide Meta-analysis. 23266556 2013
dbSNP: rs3802842
rs3802842
Entrez Id: 120376;399948
Gene Symbol: COLCA2;COLCA1
COLCA2;COLCA1
CUI: C0009402
Disease:
Colorectal Carcinoma
0.900 GeneticVariation BEFREE We identified associations at two of the six CRC susceptibility loci in MLH1 mutation carriers from the combined LS cohort: 11q23.1 (rs3802842, HR = 2.68, p ≤ 0.0001) increasing risk of CRC, and rs3802842 in a pair-wise combination with 8q23.3 (rs16892766) affecting age of diagnosis of CRC (log-rank test; p ≤ 0.0001). 22987364 2013
dbSNP: rs3802842
rs3802842
Entrez Id: 120376;399948
Gene Symbol: COLCA2;COLCA1
COLCA2;COLCA1
CUI: C0009402
Disease:
Colorectal Carcinoma
0.900 GeneticVariation BEFREE The aim of this study was to perform an association study between risk variants: rs10795668, rs16892766, rs3802842 and rs4939827 and CRC risk in Croatian population. 24066093 2013
dbSNP: rs3802842
rs3802842
Entrez Id: 120376;399948
Gene Symbol: COLCA2;COLCA1
COLCA2;COLCA1
CUI: C0007102
Disease:
Malignant tumor of colon
0.720 GeneticVariation GWASCAT Identification of Genetic Susceptibility Loci for Colorectal Tumors in a Genome-Wide Meta-analysis. 23266556 2013
dbSNP: rs3802842
rs3802842
Entrez Id: 120376;399948
Gene Symbol: COLCA2;COLCA1
COLCA2;COLCA1
CUI: C0007102
Disease:
Malignant tumor of colon
0.720 GeneticVariation BEFREE A total of 927 MMR gene mutation carriers (360 MLH1, 442 MSH2, 85 MSH6 and 40 PMS2) from 315 families enrolled in the Colon Cancer Family Registry, were genotyped for the single nucleotide polymorphisms (SNPs): rs16892766 (8q23.3), rs6983267 (8q24.21), rs719725 (9p24), rs10795668 (10p14), rs3802842 (11q23.1), rs4444235 (14q22.2), rs4779584 (15q13.3), rs9929218 (16q22.1), rs4939827 (18q21.1), rs10411210 (19q13.1) and rs961253 (20p12.3). 23434150 2013
dbSNP: rs3802842
rs3802842
Entrez Id: 120376;399948
Gene Symbol: COLCA2;COLCA1
COLCA2;COLCA1
CUI: C0346629
Disease:
Malignant neoplasm of large intestine
0.700 GeneticVariation GWASCAT Identification of Genetic Susceptibility Loci for Colorectal Tumors in a Genome-Wide Meta-analysis. 23266556 2013
dbSNP: rs3802842
rs3802842
Entrez Id: 120376;399948
Gene Symbol: COLCA2;COLCA1
COLCA2;COLCA1
CUI: C3554460
Disease:
COLORECTAL CANCER, SUSCEPTIBILITY TO, 12
0.700 GeneticVariation GWASCAT Identification of Genetic Susceptibility Loci for Colorectal Tumors in a Genome-Wide Meta-analysis. 23266556 2013
dbSNP: rs3802842
rs3802842
Entrez Id: 120376;399948
Gene Symbol: COLCA2;COLCA1
COLCA2;COLCA1
CUI: C1319315
Disease:
Adenocarcinoma of large intestine
0.700 GeneticVariation GWASCAT Identification of Genetic Susceptibility Loci for Colorectal Tumors in a Genome-Wide Meta-analysis. 23266556 2013
dbSNP: rs3802842
rs3802842
Entrez Id: 120376;399948
Gene Symbol: COLCA2;COLCA1
COLCA2;COLCA1
CUI: C2677123
Disease:
COLORECTAL CANCER, SUSCEPTIBILITY TO, 3
0.700 GeneticVariation GWASCAT Identification of Genetic Susceptibility Loci for Colorectal Tumors in a Genome-Wide Meta-analysis. 23266556 2013