Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs2294008
rs2294008
PSCA ; JRK
CUI: C0699791
Disease: Stomach Carcinoma
Stomach Carcinoma
0.800 GeneticVariation BEFREE Our study suggested rs2294008 in the PSCA gene to be associated with increased risk of gastric cancer and rs2070803 in MUC1 to play a protective role in a Chinese population. 22938426

2012

dbSNP: rs2294008
rs2294008
PSCA ; JRK
CUI: C0699791
Disease: Stomach Carcinoma
Stomach Carcinoma
0.800 GeneticVariation BEFREE Although modest limitations and potential bias cannot be eliminated, this meta-analysis suggests that PSCA -rs2294008C>T and -rs2976392G>A are potential factors of GC development for Eastern Asians, and future work may incorporate these findings and evaluate these variants as potential markers for screening and early diagnosis of GC. 22155405

2012

dbSNP: rs2294008
rs2294008
PSCA ; JRK
CUI: C0699791
Disease: Stomach Carcinoma
Stomach Carcinoma
0.800 GeneticVariation BEFREE The rs2294008 polymorphism in PSCA increases the risk of noncardia gastric cancer and its precursors in white individuals but protects against proximal cancers. 21070776

2011

dbSNP: rs2294008
rs2294008
PSCA ; JRK
CUI: C0699791
Disease: Stomach Carcinoma
Stomach Carcinoma
0.800 GeneticVariation BEFREE Our study showed that rs2294008 in the PSCA gene was associated with increased risks of gastric cancer in a Korean population, suggests that rs2294008 might play an important role in gastric carcinogenesis. 21538581

2011

dbSNP: rs2294008
rs2294008
PSCA ; JRK
CUI: C0699791
Disease: Stomach Carcinoma
Stomach Carcinoma
0.800 GeneticVariation BEFREE If validated in further studies, PSCA rs2294008</span> could be useful marker of sur</span>vival assessment and individualized clinical therapy for gastric cancer, particularly among the diffuse-type gastric cancer. 21064099

2011

dbSNP: rs2294008
rs2294008
PSCA ; JRK
CUI: C0699791
Disease: Stomach Carcinoma
Stomach Carcinoma
0.800 GeneticVariation BEFREE In conclusion, The T allele of PSCA rs2294008 is associated with increased risk of gastric cancer, especially intestinal type, poorly differentiated, early onset, and noncardia gastric cancer in Chinese population. 21268123

2011

dbSNP: rs2294008
rs2294008
PSCA ; JRK
CUI: C0699791
Disease: Stomach Carcinoma
Stomach Carcinoma
0.800 GeneticVariation BEFREE Recently, two genome-wide association studies identified a significant association between the prostate stem cell antigen (PSCA) rs2294008 (C>T) polymorphism and risk of diffuse-type of gastric cancer in Asians and bladder cancer in Caucasians, respectively. 20083643

2010

dbSNP: rs2294008
rs2294008
PSCA ; JRK
CUI: C0699791
Disease: Stomach Carcinoma
Stomach Carcinoma
0.800 GeneticVariation BEFREE Two single nucleotide polymorphisms (SNPs) (rs2976392 and rs2294008) in the PSCA gene were recently identified as the susceptibility loci of gastric cancer, especially in diffuse type. 20131315

2010

dbSNP: rs2294008
rs2294008
PSCA ; JRK
CUI: C0699791
Disease: Stomach Carcinoma
Stomach Carcinoma
0.800 GeneticVariation BEFREE The rs2294008 C/T polymorphism of the PSCA gene was significantly associated with the susceptibility to GC. 20230293

2010

dbSNP: rs2294008
rs2294008
PSCA ; JRK
CUI: C0699791
Disease: Stomach Carcinoma
Stomach Carcinoma
0.800 GeneticVariation BEFREE We found that rs2294008 and rs2976392, which were strongly linked to each other (D' = 1.00), were significantly associated with stomach cancer risk. 19582881

2009

dbSNP: rs4072037
rs4072037
CUI: C0699791
Disease: Stomach Carcinoma
Stomach Carcinoma
0.800 GeneticVariation BEFREE Our study confirms the protective effect of MUC1 rs40</span>72037 polymorphism on the risk of GC under the dominant model. 28489708

2018

dbSNP: rs4072037
rs4072037
CUI: C0699791
Disease: Stomach Carcinoma
Stomach Carcinoma
0.800 GeneticVariation BEFREE Our data suggested that rs4072037 polymorphism was associated with a decreased risk of GC. 28561882

2017

dbSNP: rs4072037
rs4072037
CUI: C0699791
Disease: Stomach Carcinoma
Stomach Carcinoma
T 0.800 GeneticVariation GWASCAT Identification of new susceptibility loci for gastric non-cardia adenocarcinoma: pooled results from two Chinese genome-wide association studies. 26701879

2017

dbSNP: rs4072037
rs4072037
CUI: C0699791
Disease: Stomach Carcinoma
Stomach Carcinoma
0.800 GeneticVariation BEFREE Published data on the association between the MUC1 rs4072037A > G polymorphism and gastric cancer (GCa) risk were inconclusive. 26910281

2016

dbSNP: rs4072037
rs4072037
CUI: C0699791
Disease: Stomach Carcinoma
Stomach Carcinoma
A 0.800 GeneticVariation GWASCAT We also confirmed a previously reported association for rs4072037 in MUC1 with p=6.59×10(-8) for total gastric cancer and similar estimates for cardia and non-cardia cancers. 26129866

2016

dbSNP: rs4072037
rs4072037
CUI: C0699791
Disease: Stomach Carcinoma
Stomach Carcinoma
0.800 GeneticVariation BEFREE Genetic variant rs4072037 of MUC1 and gastric cancer risk in an Eastern Chinese population. 26910281

2016

dbSNP: rs4072037
rs4072037
CUI: C0699791
Disease: Stomach Carcinoma
Stomach Carcinoma
0.800 GeneticVariation BEFREE Those subjects with both the risk alleles MUC1 rs9841504 and ZBTB20 rs4072037 had a greater than 3-fold increased risk of gastric cancer. 27127881

2016

dbSNP: rs4072037
rs4072037
CUI: C0699791
Disease: Stomach Carcinoma
Stomach Carcinoma
0.800 GeneticVariation GWASCAT Loss-of-function variants in ATM confer risk of gastric cancer. 26098866

2015

dbSNP: rs4072037
rs4072037
CUI: C0699791
Disease: Stomach Carcinoma
Stomach Carcinoma
0.800 GeneticVariation BEFREE Several genetic variants including PSCA rs2294008 C>T and rs2976392 G>A, MUC1 rs4072037 T>C, and PLCE1 rs2274223 A>G have shown significant association with stomach cancer risk in the previous genome-wide association studies (GWASs). 25658482

2015

dbSNP: rs4072037
rs4072037
CUI: C0699791
Disease: Stomach Carcinoma
Stomach Carcinoma
0.800 GeneticVariation BEFREE Further, subgroup analysis based on ethnicity suggested MUC1 rs4072037 polymorphism had a subtly reduced cancer risk among Asian population, and stratified analysis by cancer types showed significantly decreased risk of gastric cancer in all genetic models. 24755768

2014

dbSNP: rs4072037
rs4072037
CUI: C0699791
Disease: Stomach Carcinoma
Stomach Carcinoma
0.800 GeneticVariation BEFREE We found that the rs4072037 AG genotype was significantly associated with a reduced risk of gastric cancer [odds ratios (OR) = 0.78; 95% confidence interval (CI) = 0.67-0.91 for AG vs AA]. 24254309

2014

dbSNP: rs4072037
rs4072037
CUI: C0699791
Disease: Stomach Carcinoma
Stomach Carcinoma
0.800 GeneticVariation BEFREE The aim of this study was to determine whether rs4072037A > G in MUC1 at 1q22 and rs2274223A > G in PLCE1 at 10q23 are associated with a risk of gastric cancer in a Korean population. 24254309

2014

dbSNP: rs4072037
rs4072037
CUI: C0699791
Disease: Stomach Carcinoma
Stomach Carcinoma
0.800 GeneticVariation BEFREE Polymorphisms of PSCA (rs2976392, rs2294008) and MUC1 (rs4072037) genes are associated with GC and HRAG. 25503145

2014

dbSNP: rs4072037
rs4072037
CUI: C0699791
Disease: Stomach Carcinoma
Stomach Carcinoma
0.800 GeneticVariation BEFREE The G allele of MUC1 rs4072037 was significantly associated with a decreased risk of GC (OR = 0.72, 95 % CI 0.68-0.77; P = 7.82 × 10(-25)), as compared with A allele. 24072653

2013

dbSNP: rs4072037
rs4072037
CUI: C0699791
Disease: Stomach Carcinoma
Stomach Carcinoma
0.800 GeneticVariation BEFREE These findings indicate that the three SNPs (rs4072037, rs13361707 and rs2274223) identified in the GWASs may interact with H. pylori infection to increase the risk of GC. 24069371

2013