Source: ALL
Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs12656571
rs12656571
Entrez Id: 4124
Gene Symbol: MAN2A1
MAN2A1
CUI: C0011884
Disease:
Diabetic Retinopathy 		0.700 GeneticVariation GWASCAT Multiethnic Genome-Wide Association Study of Diabetic Retinopathy Using Liability Threshold Modeling of Duration of Diabetes and Glycemic Control. 30487263 2019
dbSNP: rs17489649
rs17489649
Entrez Id: 4124
Gene Symbol: MAN2A1
MAN2A1
CUI: C0021704
Disease:
Intelligence 		A 0.700 GeneticVariation GWASCAT A combined analysis of genetically correlated traits identifies 187 loci and a role for neurogenesis and myelination in intelligence. 29326435 2019
dbSNP: rs2300993
rs2300993
Entrez Id: 4124
Gene Symbol: MAN2A1
MAN2A1
CUI: C0011884
Disease:
Diabetic Retinopathy 		0.700 GeneticVariation GWASCAT Multiethnic Genome-Wide Association Study of Diabetic Retinopathy Using Liability Threshold Modeling of Duration of Diabetes and Glycemic Control. 30487263 2019
dbSNP: rs4388249
rs4388249
Entrez Id: 4124
Gene Symbol: MAN2A1
MAN2A1
CUI: C0036341
Disease:
Schizophrenia 		T 0.700 GeneticVariation GWASCAT Genome-Wide Association Study Detected Novel Susceptibility Genes for Schizophrenia and Shared Trans-Populations/Diseases Genetic Effect. 30285260 2019
dbSNP: rs71575306
rs71575306
Entrez Id: 4124
Gene Symbol: MAN2A1
MAN2A1
CUI: C0036341
Disease:
Schizophrenia 		0.700 GeneticVariation GWASCAT Association of Schizophrenia Risk With Disordered Niacin Metabolism in an Indian Genome-wide Association Study. 31268507 2019
dbSNP: rs13355543
rs13355543
Entrez Id: 4124
Gene Symbol: MAN2A1
MAN2A1
CUI: C0596887
Disease:
mathematical ability 		A 0.700 GeneticVariation GWASCAT Gene discovery and polygenic prediction from a genome-wide association study of educational attainment in 1.1 million individuals. 30038396 2018
dbSNP: rs1438660
rs1438660
Entrez Id: 4124
Gene Symbol: MAN2A1
MAN2A1
CUI: C0021704
Disease:
Intelligence 		A 0.700 GeneticVariation GWASCAT Genome-wide association meta-analysis in 269,867 individuals identifies new genetic and functional links to intelligence. 29942086 2018
dbSNP: rs71575306
rs71575306
Entrez Id: 4124
Gene Symbol: MAN2A1
MAN2A1
CUI: C0036341
Disease:
Schizophrenia 		0.700 GeneticVariation GWASCAT Common schizophrenia alleles are enriched in mutation-intolerant genes and in regions under strong background selection. 29483656 2018
dbSNP: rs4388249
rs4388249
Entrez Id: 4124
Gene Symbol: MAN2A1
MAN2A1
CUI: C0036341
Disease:
Schizophrenia 		T 0.700 GeneticVariation GWASCAT Genome-wide association analysis identifies 30 new susceptibility loci for schizophrenia. 28991256 2017
dbSNP: rs4388249
rs4388249
Entrez Id: 4124
Gene Symbol: MAN2A1
MAN2A1
CUI: C0036341
Disease:
Schizophrenia 		T 0.700 GeneticVariation GWASCAT Genome-wide association study of schizophrenia in Ashkenazi Jews. 26198764 2015
dbSNP: rs4388249
rs4388249
Entrez Id: 4124
Gene Symbol: MAN2A1
MAN2A1
CUI: C0036341
Disease:
Schizophrenia 		T 0.700 GeneticVariation GWASCAT Biological insights from 108 schizophrenia-associated genetic loci. 25056061 2014
dbSNP: rs2015698
rs2015698
Entrez Id: 4124
Gene Symbol: MAN2A1
MAN2A1
CUI: C0011860
Disease:
Diabetes Mellitus, Non-Insulin-Dependent 		0.010 GeneticVariation BEFREE Recent studies have explored several novel type 2 diabetes (T2D) susceptibility variants in the KCNQ1 (rs2237892), AP3S1 (rs3756555), MAN2A1 (rs2015698), and ALDH7A1 (rs2306617) genes in Japan and Western Africa. 20512086 2010
dbSNP: rs3776932
rs3776932
Entrez Id: 4124
Gene Symbol: MAN2A1
MAN2A1
CUI: C0023452
Disease:
Childhood Acute Lymphoblastic Leukemia 		0.010 GeneticVariation BEFREE Of these 1 million SNPs, six SNPs in 4 genes (HAO1 rs6140264, EPB41L2 rs9388856, rs9388857, rs1360756, C2orf3 12105972, MAN2A1 rs3776932) were strongly associated with childhood ALL risk (P(dominant)<or=0.0001 and P(trend)<0.006). 20189245 2010