Source: ALL
Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs1304029
rs1304029
Entrez Id: 135152
Gene Symbol: B3GAT2
B3GAT2
CUI: C1861172
Disease:
Venous Thromboembolism 		0.700 GeneticVariation GWASCAT Rare genetic variants in SMAP1, B3GAT2, and RIMS1 contribute to pediatric venous thromboembolism. 28011674 2017
dbSNP: rs10945275
rs10945275
Entrez Id: 135152
Gene Symbol: B3GAT2
B3GAT2
CUI: C0036341
Disease:
Schizophrenia 		0.010 GeneticVariation BEFREE A second SNP (r(2) = .24 with rs10945275), which conferred the highest SCZ risk effect in the Norwegian subset, was also associated with cortical area. 20950796 2011
dbSNP: rs2460691
rs2460691
Entrez Id: 135152;105377850
Gene Symbol: B3GAT2;LOC105377850
B3GAT2;LOC105377850
CUI: C0036341
Disease:
Schizophrenia 		0.010 GeneticVariation BEFREE Increased dosage of the rs2460691 SCZ risk allele was associated with decreased cortical area (p = .002) but not thickness or hippocampal volume. 20950796 2011