rs9606756, TCN2

N. diseases: 7
Disease: Anemia, Pernicious ×
Source: ALL
Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
Anemia, Pernicious
CUI: C0002892
Disease: Anemia, Pernicious
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