B3GALT1, beta-1,3-galactosyltransferase 1, 8708

N. diseases: 3; N. variants: 6
Source: ALL
Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs79827531
rs79827531
Entrez Id: 8708
Gene Symbol: B3GALT1
B3GALT1
CUI: C0003467
Disease:
Anxiety 		A 0.700 GeneticVariation GWASCAT Meta-analysis of genome-wide association studies for neuroticism in 449,484 individuals identifies novel genetic loci and pathways. 29942085 2018
dbSNP: rs10200961
rs10200961
Entrez Id: 8708;105616981
Gene Symbol: B3GALT1;B3GALT1-AS1
B3GALT1;B3GALT1-AS1
CUI: C0023467
Disease:
Leukemia, Myelocytic, Acute 		G 0.700 GeneticVariation GWASCAT Genome-wide haplotype association study identify the FGFR2 gene as a risk gene for acute myeloid leukemia. 27903959 2017
dbSNP: rs10200961
rs10200961
Entrez Id: 8708;105616981
Gene Symbol: B3GALT1;B3GALT1-AS1
B3GALT1;B3GALT1-AS1
CUI: C0023467
Disease:
Leukemia, Myelocytic, Acute 		A 0.700 GeneticVariation GWASCAT Genome-wide haplotype association study identify the FGFR2 gene as a risk gene for acute myeloid leukemia. 27903959 2017
dbSNP: rs16854287
rs16854287
Entrez Id: 8708;105616981
Gene Symbol: B3GALT1;B3GALT1-AS1
B3GALT1;B3GALT1-AS1
CUI: C0023467
Disease:
Leukemia, Myelocytic, Acute 		C 0.700 GeneticVariation GWASCAT Genome-wide haplotype association study identify the FGFR2 gene as a risk gene for acute myeloid leukemia. 27903959 2017
dbSNP: rs75904417
rs75904417
Entrez Id: 8708
Gene Symbol: B3GALT1
B3GALT1
CUI: C2697787
Disease:
Interleukin 7 Measurement 		C 0.700 GeneticVariation GWASCAT Genome-wide Association Study Identifies 27 Loci Influencing Concentrations of Circulating Cytokines and Growth Factors. 27989323 2017
dbSNP: rs116677506
rs116677506
Entrez Id: 8708
Gene Symbol: B3GALT1
B3GALT1
CUI: C0002395
Disease:
Alzheimer's Disease 		A 0.700 GeneticVariation GWASCAT Family-based association analyses of imputed genotypes reveal genome-wide significant association of Alzheimer's disease with OSBPL6, PTPRG, and PDCL3. 26830138 2016
dbSNP: rs971257
rs971257
Entrez Id: 8708
Gene Symbol: B3GALT1
B3GALT1
CUI: C0004352
Disease:
Autistic Disorder 		0.010 GeneticVariation BEFREE We also found evidence for association between autism and two other SNPs (rs1517342, P = 0.012 and rs971257, P = 0.030) or haplotypes (P = 0.003) of the STK39 gene. 18348195 2008