TCN1, transcobalamin 1, 6947

N. diseases: 52; N. variants: 4
Source: ALL
Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs526934
rs526934
Entrez Id: 6947
Gene Symbol: TCN1
TCN1
CUI: C0202252
Disease:
VITAMIN B12 MEASUREMENT 		0.800 GeneticVariation GWASDB Genome-wide significant predictors of metabolites in the one-carbon metabolism pathway. 19744961 2009
dbSNP: rs526934
rs526934
Entrez Id: 6947
Gene Symbol: TCN1
TCN1
CUI: C0202252
Disease:
VITAMIN B12 MEASUREMENT 		0.800 GeneticVariation GWASCAT Genome-wide significant predictors of metabolites in the one-carbon metabolism pathway. 19744961 2009
dbSNP: rs34324219
rs34324219
Entrez Id: 6947
Gene Symbol: TCN1
TCN1
CUI: C2985280
Disease:
Blood Protein Measurement 		A 0.700 GeneticVariation GWASCAT Genomic atlas of the human plasma proteome. 29875488 2018
dbSNP: rs34528912
rs34528912
Entrez Id: 6947
Gene Symbol: TCN1
TCN1
CUI: C2985280
Disease:
Blood Protein Measurement 		T 0.700 GeneticVariation GWASCAT Genomic atlas of the human plasma proteome. 29875488 2018
dbSNP: rs34324219
rs34324219
Entrez Id: 6947
Gene Symbol: TCN1
TCN1
CUI: C0202252
Disease:
VITAMIN B12 MEASUREMENT 		A 0.700 GeneticVariation GWASCAT GWAS identifies population-specific new regulatory variants in FUT6 associated with plasma B12 concentrations in Indians. 28334792 2017
dbSNP: rs34324219
rs34324219
Entrez Id: 6947
Gene Symbol: TCN1
TCN1
CUI: C0202252
Disease:
VITAMIN B12 MEASUREMENT 		A 0.700 GeneticVariation GWASCAT Genetic Associations with Plasma B12, B6, and Folate Levels in an Ischemic Stroke Population from the Vitamin Intervention for Stroke Prevention (VISP) Trial. 25147783 2014
dbSNP: rs1209702636
rs1209702636
Entrez Id: 6947
Gene Symbol: TCN1
TCN1
CUI: C0342700
Disease:
Transcobalamin I Deficiency 		T 0.700 CausalMutation CLINVAR
dbSNP: rs526934
rs526934
Entrez Id: 6947
Gene Symbol: TCN1
TCN1
CUI: C0024623
Disease:
Malignant neoplasm of stomach 		0.010 GeneticVariation BEFREE The variant rs526934 from the TCN1 gene was associated with an increased risk of developing gastric cancer. 26959381 2016
dbSNP: rs526934
rs526934
Entrez Id: 6947
Gene Symbol: TCN1
TCN1
CUI: C0699791
Disease:
Stomach Carcinoma 		0.010 GeneticVariation BEFREE The variant rs526934 from the TCN1 gene was associated with an increased risk of developing gastric cancer. 26959381 2016