Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs10411210
rs10411210
CUI: C0009402
Disease: Colorectal Carcinoma
Colorectal Carcinoma
C 0.840 GeneticVariation GWASCAT Novel Common Genetic Susceptibility Loci for Colorectal Cancer. 29917119

2019

dbSNP: rs10411210
rs10411210
CUI: C0009402
Disease: Colorectal Carcinoma
Colorectal Carcinoma
C 0.840 GeneticVariation GWASCAT Large-Scale Genome-Wide Association Study of East Asians Identifies Loci Associated With Risk for Colorectal Cancer. 30529582

2019

dbSNP: rs10411210
rs10411210
CUI: C0009402
Disease: Colorectal Carcinoma
Colorectal Carcinoma
0.840 GeneticVariation BEFREE In addition, a variant previously identified through fine-mapping in this GWAS in the region 19q13.1, rs7252505, was confirmed to be more strongly associated with CRC in the African American replication set than the variant originally reported in Europeans (rs10411210). 28295283

2017

dbSNP: rs10411210
rs10411210
CUI: C0009402
Disease: Colorectal Carcinoma
Colorectal Carcinoma
0.840 GeneticVariation BEFREE Among the 22 SNPs, two (rs1321311G>T in CDKN1A and rs10411210C>T in RHPN2) were significantly associated with the survival outcomes of CRC in a multivariate survival analysis. 25799222

2015

dbSNP: rs10411210
rs10411210
CUI: C0009402
Disease: Colorectal Carcinoma
Colorectal Carcinoma
0.840 GeneticVariation BEFREE Collectively, our analysis further highlights significant association bet</span>ween rs10411210 polymorphism and colorectal cancer. 26349980

2015

dbSNP: rs10411210
rs10411210
CUI: C0009402
Disease: Colorectal Carcinoma
Colorectal Carcinoma
0.840 GeneticVariation BEFREE The present results suggest that the genetic variants of the CDKN1A (rs1321311) and RHPN2 (rs10411210) genes can be used as prognostic biomarkers for patients with surgically resected colorectal cancer. 25799222

2015

dbSNP: rs10411210
rs10411210
CUI: C0009402
Disease: Colorectal Carcinoma
Colorectal Carcinoma
0.840 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: rs10411210
rs10411210
CUI: C0009402
Disease: Colorectal Carcinoma
Colorectal Carcinoma
C 0.840 GeneticVariation GWASCAT We identified four previously unreported CRC risk loci at 14q22.2 (rs4444235, BMP4; P = 8.1 x 10(-10)), 16q22.1 (rs9929218, CDH1; P = 1.2 x 10(-8)), 19q13.1 (rs10411210, RHPN2; P = 4.6 x 10(-9)) and 20p12.3 (rs961253; P = 2.0 x 10(-10)). 19011631

2008

dbSNP: rs10411210
rs10411210
CUI: C0009402
Disease: Colorectal Carcinoma
Colorectal Carcinoma
C 0.840 GeneticVariation GWASDB We identified four previously unreported CRC risk loci at 14q22.2 (rs4444235, BMP4; P = 8.1 x 10(-10)), 16q22.1 (rs9929218, CDH1; P = 1.2 x 10(-8)), 19q13.1 (rs10411210, RHPN2; P = 4.6 x 10(-9)) and 20p12.3 (rs961253; P = 2.0 x 10(-10)). 19011631

2008