Source: CURATED

Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs10049390
rs10049390
SLCO2A1
CUI: C0009402
Disease: Colorectal Carcinoma
Colorectal Carcinoma 		A 0.700 GeneticVariation GWASCAT Discovery of common and rare genetic risk variants for colorectal cancer. 30510241

2019
dbSNP: rs1011970
rs1011970
CDKN2B-AS1
CUI: C0009402
Disease: Colorectal Carcinoma
Colorectal Carcinoma 		T 0.700 GeneticVariation GWASCAT Cross-Cancer Genome-Wide Analysis of Lung, Ovary, Breast, Prostate, and Colorectal Cancer Reveals Novel Pleiotropic Associations. 27197191

2016
dbSNP: rs10152518
rs10152518
CUI: C0009402
Disease: Colorectal Carcinoma
Colorectal Carcinoma 		G 0.700 GeneticVariation GWASCAT Association analyses identify 31 new risk loci for colorectal cancer susceptibility. 31089142

2019
dbSNP: rs1023890
rs1023890
CUI: C0009402
Disease: Colorectal Carcinoma
Colorectal Carcinoma 		A 0.700 GeneticVariation GWASDB A colorectal cancer susceptibility new variant at 4q26 in the Spanish population identified by genome-wide association analysis. 24978480

2014
dbSNP: rs1028166
rs1028166
TENM3 ; TENM3-AS1
CUI: C0009402
Disease: Colorectal Carcinoma
Colorectal Carcinoma 		G 0.700 GeneticVariation GWASCAT No evidence of gene-calcium interactions from genome-wide analysis of colorectal cancer risk. 25192705

2014
dbSNP: rs10414971
rs10414971
ZNF442
CUI: C0009402
Disease: Colorectal Carcinoma
Colorectal Carcinoma 		0.700 GeneticVariation UNIPROT

dbSNP: rs1043397364
rs1043397364
DPEP1
CUI: C0009402
Disease: Colorectal Carcinoma
Colorectal Carcinoma 		0.700 GeneticVariation UNIPROT

dbSNP: rs10457678
rs10457678
ECT2L
CUI: C0009402
Disease: Colorectal Carcinoma
Colorectal Carcinoma 		A 0.700 GeneticVariation GWASCAT Meta-analysis of genome-wide association studies identifies common susceptibility polymorphisms for colorectal and endometrial cancer near SH2B3 and TSHZ1. 26621817

2015
dbSNP: rs10511330
rs10511330
ZBTB20
CUI: C0009402
Disease: Colorectal Carcinoma
Colorectal Carcinoma 		C 0.700 GeneticVariation GWASCAT Associations of single nucleotide polymorphisms with mucinous colorectal cancer: genome-wide common variant and gene-based rare variant analyses. 29942513

2018
dbSNP: rs1057519365
rs1057519365
BRIP1
CUI: C0009402
Disease: Colorectal Carcinoma
Colorectal Carcinoma 		A 0.700 GeneticVariation CLINVAR The Fanconi anemia DNA damage repair pathway in the spotlight for germline predisposition to colorectal cancer. 27165003

2016
dbSNP: rs1057519366
rs1057519366
FANCC
CUI: C0009402
Disease: Colorectal Carcinoma
Colorectal Carcinoma 		AG 0.700 GeneticVariation CLINVAR The Fanconi anemia DNA damage repair pathway in the spotlight for germline predisposition to colorectal cancer. 27165003

2016
dbSNP: rs1057519367
rs1057519367
REV3L ; MFSD4B
CUI: C0009402
Disease: Colorectal Carcinoma
Colorectal Carcinoma 		A 0.700 GeneticVariation CLINVAR The Fanconi anemia DNA damage repair pathway in the spotlight for germline predisposition to colorectal cancer. 27165003

2016
dbSNP: rs1057519739
rs1057519739
SMAD4
CUI: C0009402
Disease: Colorectal Carcinoma
Colorectal Carcinoma 		0.700 GeneticVariation UNIPROT

dbSNP: rs1057519895
rs1057519895
FBXW7
CUI: C0009402
Disease: Colorectal Carcinoma
Colorectal Carcinoma 		0.700 GeneticVariation UNIPROT

dbSNP: rs1057519925
rs1057519925
PIK3CA
CUI: C0009402
Disease: Colorectal Carcinoma
Colorectal Carcinoma 		0.700 GeneticVariation UNIPROT

dbSNP: rs1057519930
rs1057519930
PIK3CA
CUI: C0009402
Disease: Colorectal Carcinoma
Colorectal Carcinoma 		0.700 GeneticVariation UNIPROT

dbSNP: rs1057520038
rs1057520038
STK11
CUI: C0009402
Disease: Colorectal Carcinoma
Colorectal Carcinoma 		0.700 GeneticVariation UNIPROT

dbSNP: rs1057941
rs1057941
GBAP1
CUI: C0009402
Disease: Colorectal Carcinoma
Colorectal Carcinoma 		A 0.700 GeneticVariation GWASCAT Cross-Cancer Genome-Wide Analysis of Lung, Ovary, Breast, Prostate, and Colorectal Cancer Reveals Novel Pleiotropic Associations. 27197191

2016
dbSNP: rs10749971
rs10749971
LOC105369491
CUI: C0009402
Disease: Colorectal Carcinoma
Colorectal Carcinoma 		0.700 GeneticVariation GWASDB Meta-analysis of genome-wide association data identifies four new susceptibility loci for colorectal cancer. 19011631

2008
dbSNP: rs1078643
rs1078643
TMEM238L ; TMEM220-AS1
CUI: C0009402
Disease: Colorectal Carcinoma
Colorectal Carcinoma 		A 0.700 GeneticVariation GWASCAT Large-Scale Genome-Wide Association Study of East Asians Identifies Loci Associated With Risk for Colorectal Cancer. 30529582

2019
dbSNP: rs1078643
rs1078643
TMEM238L ; TMEM220-AS1
CUI: C0009402
Disease: Colorectal Carcinoma
Colorectal Carcinoma 		A 0.700 GeneticVariation GWASCAT Discovery of common and rare genetic risk variants for colorectal cancer. 30510241

2019
dbSNP: rs1078643
rs1078643
TMEM238L ; TMEM220-AS1
CUI: C0009402
Disease: Colorectal Carcinoma
Colorectal Carcinoma 		A 0.700 GeneticVariation GWASCAT Association analyses identify 31 new risk loci for colorectal cancer susceptibility. 31089142

2019
dbSNP: rs10808555
rs10808555
POU5F1B ; CASC8 ; PCAT1
CUI: C0009402
Disease: Colorectal Carcinoma
Colorectal Carcinoma 		0.700 GeneticVariation GWASDB Meta-analysis of genome-wide association data identifies four new susceptibility loci for colorectal cancer. 19011631

2008
dbSNP: rs10821907
rs10821907
CUI: C0009402
Disease: Colorectal Carcinoma
Colorectal Carcinoma 		C 0.700 GeneticVariation GWASCAT Discovery of common and rare genetic risk variants for colorectal cancer. 30510241

2019
dbSNP: rs10849433
rs10849433
LOC105369624
CUI: C0009402
Disease: Colorectal Carcinoma
Colorectal Carcinoma 		C 0.700 GeneticVariation GWASCAT Discovery of common and rare genetic risk variants for colorectal cancer. 30510241

2019