Source: ALL
Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs12424113
rs12424113
Entrez Id: 283358
Gene Symbol: B4GALNT3
B4GALNT3
CUI: C0005890
Disease:
Body Height 		0.700 GeneticVariation GWASCAT Characterizing rare and low-frequency height-associated variants in the Japanese population. 31562340 2019
dbSNP: rs12811171
rs12811171
Entrez Id: 283358
Gene Symbol: B4GALNT3
B4GALNT3
CUI: C0005890
Disease:
Body Height 		0.700 GeneticVariation GWASCAT Leveraging Polygenic Functional Enrichment to Improve GWAS Power. 30595370 2019
dbSNP: rs34716573
rs34716573
Entrez Id: 283358
Gene Symbol: B4GALNT3
B4GALNT3
CUI: C0424621
Disease:
Body Fat Distribution 		C 0.700 GeneticVariation GWASCAT Genome-wide association study of body fat distribution identifies adiposity loci and sex-specific genetic effects. 30664634 2019
dbSNP: rs6489548
rs6489548
Entrez Id: 283358
Gene Symbol: B4GALNT3
B4GALNT3
CUI: C0005890
Disease:
Body Height 		0.700 GeneticVariation GWASCAT Characterizing rare and low-frequency height-associated variants in the Japanese population. 31562340 2019
dbSNP: rs11063544
rs11063544
Entrez Id: 283358
Gene Symbol: B4GALNT3
B4GALNT3
CUI: C0410702
Disease:
Adolescent idiopathic scoliosis 		0.700 GeneticVariation GWASCAT The coexistence of copy number variations (CNVs) and single nucleotide polymorphisms (SNPs) at a locus can result in distorted calculations of the significance in associating SNPs to disease. 30019117 2018
dbSNP: rs11063544
rs11063544
Entrez Id: 283358
Gene Symbol: B4GALNT3
B4GALNT3
CUI: C1837461
Disease:
SCOLIOSIS, ISOLATED, SUSCEPTIBILITY TO, 3 		0.700 GeneticVariation GWASCAT The coexistence of copy number variations (CNVs) and single nucleotide polymorphisms (SNPs) at a locus can result in distorted calculations of the significance in associating SNPs to disease. 30019117 2018
dbSNP: rs143741106
rs143741106
Entrez Id: 283358
Gene Symbol: B4GALNT3
B4GALNT3
CUI: C2985280
Disease:
Blood Protein Measurement 		C 0.700 GeneticVariation GWASCAT Genomic atlas of the human plasma proteome. 29875488 2018
dbSNP: rs7298766
rs7298766
Entrez Id: 283358
Gene Symbol: B4GALNT3
B4GALNT3
CUI: C2985280
Disease:
Blood Protein Measurement 		G 0.700 GeneticVariation GWASCAT Genomic atlas of the human plasma proteome. 29875488 2018
dbSNP: rs7966590
rs7966590
Entrez Id: 283358
Gene Symbol: B4GALNT3
B4GALNT3
CUI: C0201850
Disease:
Alkaline phosphatase measurement 		0.700 GeneticVariation GWASCAT Genetic analysis of quantitative traits in the Japanese population links cell types to complex human diseases. 29403010 2018
dbSNP: rs12811171
rs12811171
Entrez Id: 283358
Gene Symbol: B4GALNT3
B4GALNT3
CUI: C0005890
Disease:
Body Height 		T 0.700 GeneticVariation GWASCAT Whole-Genome Sequencing Coupled to Imputation Discovers Genetic Signals for Anthropometric Traits. 28552196 2017
dbSNP: rs11612228
rs11612228
Entrez Id: 283358
Gene Symbol: B4GALNT3
B4GALNT3
CUI: C0005890
Disease:
Body Height 		T 0.700 GeneticVariation GWASCAT Defining the role of common variation in the genomic and biological architecture of adult human height. 25282103 2014