Variant Gene Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs3760776
rs3760776
0.010 GeneticVariation BEFREE FUT6 (rs3760776) AA genotype was present in four (4.8%) autoimmune gastritis patients (all pernicious anaemia) and three (1.7%) controls (p = 0.007). 25681243

2015

dbSNP: rs9606756
rs9606756
0.010 GeneticVariation BEFREE TCN2 (rs9606756) GG genotype, related with lower vitamin B12 levels, was found in 3 (3.6%) autoimmune gastritis patients (2 with pernicious anaemia), but in none of controls (p = 0.02). 25681243

2015

dbSNP: rs1799945
rs1799945
0.010 GeneticVariation BEFREE The son of our patient was compound C282Y/H63D heterozygous without detectable pernicious anaemia. 18176074

2008

dbSNP: rs1801198
rs1801198
0.010 GeneticVariation BEFREE The patient was heterozygous for the transcobalamin (TC) II polymorphism 776C --> G. This case demonstrates the importance of functional assessment of intracellular B12 activity (e.g. serum homocysteine) in excluding B12 deficiency, the role of steroids in pernicious anaemia and a possible clinical correlation of a TCII polymorphism. 16343274

2006