Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs505922
rs505922
Entrez Id: 28
Gene Symbol: ABO
ABO
CUI: C0006826
Disease:
Malignant Neoplasms
0.020 GeneticVariation BEFREE This study provided evidence of SNP rs505922 C allele as a strong risk factor of cancer susceptibility, specifically for pancreatic cancer. 25656610 2015
dbSNP: rs505922
rs505922
Entrez Id: 28
Gene Symbol: ABO
ABO
CUI: C0006826
Disease:
Malignant Neoplasms
0.020 GeneticVariation BEFREE Carriers of the C allele of rs505922 had an increased cancer risk [adjusted odds ratio (OR) = 1.42, 95% confidence interval (CI): 1.02-1.98] compared to TT carriers. 23816557 2014