rs9606756, TCN2

N. diseases: 7
Source: ALL
Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
Crohn Disease
CUI: C0010346
Disease: Crohn Disease
0.010 GeneticVariation BEFREE TCN2 (rs1801198, rs9606756) polymorphisms as well as folate deficiency and vitamin B12 deficiency are correlated with CD. 28472811 2017
Folic Acid Deficiency
CUI: C0016412
Disease: Folic Acid Deficiency
0.010 GeneticVariation BEFREE TCN2 (rs1801198, rs9606756) polymorphisms as well as folate deficiency and vitamin B12 deficiency are correlated with CD. 28472811 2017
Vitamin B 12 Deficiency
CUI: C0042847
Disease: Vitamin B 12 Deficiency
0.010 GeneticVariation BEFREE TCN2 (rs1801198, rs9606756) polymorphisms as well as folate deficiency and vitamin B12 deficiency are correlated with CD. 28472811 2017
Ulcerative Colitis
CUI: C0009324
Disease: Ulcerative Colitis
0.010 GeneticVariation BEFREE TCN2 (rs1801198, rs9606756) mutations might aggravate the severity of UC. 28526947 2017
Obesity
CUI: C0028754
Disease: Obesity
0.010 GeneticVariation BEFREE The TCN2 variant of rs9606756 [Ile23Val] acts as risk loci for obesity-related traits and mediates by interacting with Apo-A1. 28417558 2017
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
Autoimmune gastritis
CUI: C3887639
Disease: Autoimmune gastritis
0.010 GeneticVariation BEFREE A genetic variant of TCN2 (rs9606756) related to lower vitamin B12 levels was more frequent in pernicious anaemia patients compared to controls, showing the plausibility of genetic factors determining the possible clinical manifestation of autoimmune gastritis. 25681243 2015