Disease: Malignant neoplasm of stomach ×
Source: ALL
Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs16901946
rs16901946
Entrez Id: 100750225;101867536;103021165
Gene Symbol: PCAT1;PRNCR1;CASC19
PCAT1;PRNCR1;CASC19
CUI: C0024623
Disease:
Malignant neoplasm of stomach 		0.020 GeneticVariation BEFREE In the recessive model, the rs16901946 GG genotype was associated with decreased risk of GC and IGC in males aged ≥60 years. 31288430 2019
dbSNP: rs16901946
rs16901946
Entrez Id: 100750225;101867536;103021165
Gene Symbol: PCAT1;PRNCR1;CASC19
PCAT1;PRNCR1;CASC19
CUI: C0024623
Disease:
Malignant neoplasm of stomach 		0.020 GeneticVariation BEFREE <b>Conclusions:</b> Our study suggested that rs16</span>901946 G allele carriers have an increased risk of gastric cancer, and the risk could be enhanced by the interactions between the polymorphism and age, sex, <i>Helicobacter pylori</i> infection. 28367233 2017
dbSNP: rs1016343
rs1016343
Entrez Id: 100750225;101867536;103021165;103164619
Gene Symbol: PCAT1;PRNCR1;CASC19;PCAT2
PCAT1;PRNCR1;CASC19;PCAT2
CUI: C0024623
Disease:
Malignant neoplasm of stomach 		0.010 GeneticVariation BEFREE In the stratification analyses, the recessive model indicated that the rs1016343 TT genotype was significantly associated with decreased GC risk in individuals aged <60 years showing lymph node metastasis (LNM)-negative results. 31288430 2019
dbSNP: rs13252298
rs13252298
Entrez Id: 100750225;101867536;103021165;103164619
Gene Symbol: PCAT1;PRNCR1;CASC19;PCAT2
PCAT1;PRNCR1;CASC19;PCAT2
CUI: C0024623
Disease:
Malignant neoplasm of stomach 		0.010 GeneticVariation BEFREE The rs13252298 GG genotype in the recessive model showed increased GC risk in subjects aged ≥60 years showing LNM-positive results and those aged ≥60 years in tumor stage III. 31288430 2019