Source: ALL
Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs11763876
rs11763876
Entrez Id: 56913
Gene Symbol: C1GALT1
C1GALT1
CUI: C0011860
Disease:
Diabetes Mellitus, Non-Insulin-Dependent 		0.700 GeneticVariation GWASCAT Leveraging Polygenic Functional Enrichment to Improve GWAS Power. 30595370 2019
dbSNP: rs11771259
rs11771259
Entrez Id: 56913
Gene Symbol: C1GALT1
C1GALT1
CUI: C0007222
Disease:
Cardiovascular Diseases 		0.700 GeneticVariation GWASCAT Leveraging Polygenic Functional Enrichment to Improve GWAS Power. 30595370 2019
dbSNP: rs11771259
rs11771259
Entrez Id: 56913
Gene Symbol: C1GALT1
C1GALT1
CUI: C0005823
Disease:
Blood Pressure 		0.700 GeneticVariation GWASCAT Genetic overlap of chronic obstructive pulmonary disease and cardiovascular disease-related traits: a large-scale genome-wide cross-trait analysis. 30940143 2019
dbSNP: rs11771259
rs11771259
Entrez Id: 56913
Gene Symbol: C1GALT1
C1GALT1
CUI: C0024117
Disease:
Chronic Obstructive Airway Disease 		0.700 GeneticVariation GWASCAT Genetic overlap of chronic obstructive pulmonary disease and cardiovascular disease-related traits: a large-scale genome-wide cross-trait analysis. 30940143 2019
dbSNP: rs4318980
rs4318980
Entrez Id: 56913
Gene Symbol: C1GALT1
C1GALT1
CUI: C0016529
Disease:
Forced expiratory volume function 		A 0.700 GeneticVariation GWASCAT New genetic signals for lung function highlight pathways and chronic obstructive pulmonary disease associations across multiple ancestries. 30804560 2019
dbSNP: rs4318980
rs4318980
Entrez Id: 56913
Gene Symbol: C1GALT1
C1GALT1
CUI: C1518922
Disease:
peak expiratory flow (procedure) 		A 0.700 GeneticVariation GWASCAT New genetic signals for lung function highlight pathways and chronic obstructive pulmonary disease associations across multiple ancestries. 30804560 2019
dbSNP: rs7787942
rs7787942
Entrez Id: 56913
Gene Symbol: C1GALT1
C1GALT1
CUI: C2985280
Disease:
Blood Protein Measurement 		T 0.700 GeneticVariation GWASCAT Genomic atlas of the human plasma proteome. 29875488 2018
dbSNP: rs1047763
rs1047763
Entrez Id: 56913
Gene Symbol: C1GALT1
C1GALT1
CUI: C0017661
Disease:
IGA Glomerulonephritis 		0.010 GeneticVariation BEFREE The rs1047763 SNP of the C1GALT1 gene probably has no correlation with genetic susceptibility to IgAN in Xinjiang Uyghur people. 26782518 2015
dbSNP: rs5882115
rs5882115
Entrez Id: 56913
Gene Symbol: C1GALT1
C1GALT1
CUI: C0017661
Disease:
IGA Glomerulonephritis 		0.010 GeneticVariation BEFREE The frequencies of the I allele and DI genotype of rs5882115 in IgAN patients were significantly higher than those in controls (P < 0.05). 26125729 2015
dbSNP: rs761991666
rs761991666
Entrez Id: 56913
Gene Symbol: C1GALT1
C1GALT1
CUI: C0017661
Disease:
IGA Glomerulonephritis 		0.010 GeneticVariation BEFREE Our previous study has shown a potential interaction of C1GALT1-330G/T and IL5RA31 + 197A/G on the susceptibility of IgAN in Southern Han Chinese. 24271554 2014
dbSNP: rs1008898
rs1008898
Entrez Id: 56913
Gene Symbol: C1GALT1
C1GALT1
CUI: C0017661
Disease:
IGA Glomerulonephritis 		0.010 GeneticVariation BEFREE C1GALT1 showed an association with IgAN (rs1008898: P = 0.0019 and rs7790522: P = 0.0049). 22131235 2012
dbSNP: rs1047763
rs1047763
Entrez Id: 56913
Gene Symbol: C1GALT1
C1GALT1
CUI: C0017658
Disease:
Glomerulonephritis 		0.010 GeneticVariation BEFREE Therefore, we analysed the distribution of the functional MCP-1 -2518 A > G (rs 1024611) and 1 beta 1,3-galactosyltransferase (C1GalT1) 1365 A > G (rs1047763) polymorphic variants in patients with primary GN (n = 144) and controls (n = 437) in a sample of the Polish population. 22203484 2012
dbSNP: rs7790522
rs7790522
Entrez Id: 56913
Gene Symbol: C1GALT1
C1GALT1
CUI: C0017661
Disease:
IGA Glomerulonephritis 		0.010 GeneticVariation BEFREE C1GALT1 showed an association with IgAN (rs1008898: P = 0.0019 and rs7790522: P = 0.0049). 22131235 2012