Source: ALL
Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs4949718
rs4949718
Entrez Id: 256435
Gene Symbol: ST6GALNAC3
ST6GALNAC3
CUI: C0201836
Disease:
Alanine aminotransferase measurement 		A 0.800 GeneticVariation GWASDB Genome-wide association study of liver enzymes in korean children. 24124411 2013
dbSNP: rs4949718
rs4949718
Entrez Id: 256435
Gene Symbol: ST6GALNAC3
ST6GALNAC3
CUI: C0201836
Disease:
Alanine aminotransferase measurement 		A 0.800 GeneticVariation GWASCAT Genome-wide association study of liver enzymes in korean children. 24124411 2013
dbSNP: rs4949718
rs4949718
Entrez Id: 256435
Gene Symbol: ST6GALNAC3
ST6GALNAC3
CUI: C1883008
Disease:
Serum Alanine Aminotransferase Measurement 		A 0.800 GeneticVariation GWASDB Genome-wide association study of liver enzymes in korean children. 24124411 2013
dbSNP: rs4949718
rs4949718
Entrez Id: 256435
Gene Symbol: ST6GALNAC3
ST6GALNAC3
CUI: C1883008
Disease:
Serum Alanine Aminotransferase Measurement 		A 0.800 GeneticVariation GWASCAT Genome-wide association study of liver enzymes in korean children. 24124411 2013
dbSNP: rs10782606
rs10782606
Entrez Id: 256435
Gene Symbol: ST6GALNAC3
ST6GALNAC3
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: rs10782606
rs10782606
Entrez Id: 256435
Gene Symbol: ST6GALNAC3
ST6GALNAC3
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: rs2631781
rs2631781
Entrez Id: 256435
Gene Symbol: ST6GALNAC3
ST6GALNAC3
CUI: C3894553
Disease:
response to simvastatin 		0.700 GeneticVariation GWASCAT Genetic Variants in HSD17B3, SMAD3, and IPO11 Impact Circulating Lipids in Response to Fenofibrate in Individuals With Type 2 Diabetes. 28736931 2018
dbSNP: rs2631781
rs2631781
Entrez Id: 256435
Gene Symbol: ST6GALNAC3
ST6GALNAC3
CUI: C0011860
Disease:
Diabetes Mellitus, Non-Insulin-Dependent 		0.700 GeneticVariation GWASCAT Genetic Variants in HSD17B3, SMAD3, and IPO11 Impact Circulating Lipids in Response to Fenofibrate in Individuals With Type 2 Diabetes. 28736931 2018
dbSNP: rs4949718
rs4949718
Entrez Id: 256435
Gene Symbol: ST6GALNAC3
ST6GALNAC3
CUI: C0201899
Disease:
Aspartate aminotransferase measurement 		A 0.700 GeneticVariation GWASCAT Genome-wide association study of liver enzymes in korean children. 24124411 2013
dbSNP: rs915404
rs915404
Entrez Id: 256435
Gene Symbol: ST6GALNAC3
ST6GALNAC3
CUI: C2700366
Disease:
Adiponectin Measurement 		0.700 GeneticVariation GWASDB Adiponectin concentrations: a genome-wide association study. 20887962 2010
dbSNP: rs12239582
rs12239582
Entrez Id: 256435
Gene Symbol: ST6GALNAC3
ST6GALNAC3
CUI: C0678222
Disease:
Breast Carcinoma 		0.010 GeneticVariation BEFREE Heterozygotes of one SNP (rs12239582) were found to have a statistically significant association with a low risk of breast cancer (OR 0.82, 95% CI 0.68-0.99), and minor homozygotes of the same SNP were found to have a tendency towards a low risk of being in the group with low vitamin D levels (OR 0.72, 95% CI 0.52-1.00). 29291743 2018
dbSNP: rs12239582
rs12239582
Entrez Id: 256435
Gene Symbol: ST6GALNAC3
ST6GALNAC3
CUI: C0006142
Disease:
Malignant neoplasm of breast 		0.010 GeneticVariation BEFREE Heterozygotes of one SNP (rs12239582) were found to have a statistically significant association with a low risk of breast cancer (OR 0.82, 95% CI 0.68-0.99), and minor homozygotes of the same SNP were found to have a tendency towards a low risk of being in the group with low vitamin D levels (OR 0.72, 95% CI 0.52-1.00). 29291743 2018
dbSNP: rs10873876
rs10873876
Entrez Id: 256435
Gene Symbol: ST6GALNAC3
ST6GALNAC3
CUI: C0023467
Disease:
Leukemia, Myelocytic, Acute 		0.010 GeneticVariation BEFREE However, the variant T allele of rs10873876 decreased the AML risk, which was in the opposite effect direction (OR 0.62, P < 0.001 in additive model). 26177813 2016