IGF2, insulin like growth factor 2, 3481

N. diseases: 604; N. variants: 19
Source: ALL
Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs1004446
rs1004446
Entrez Id: 3481;51214;723961
Gene Symbol: IGF2;IGF2-AS;INS-IGF2
IGF2;IGF2-AS;INS-IGF2
CUI: C0011854
Disease:
Diabetes Mellitus, Insulin-Dependent 		0.810 GeneticVariation BEFREE Characteristics included are age at multiple autoantibody positivity, sex, selected high-risk HLA-DR-DQ genotypes, relationship to a family member with T1D, autoantibody at seroconversion, <i>INS</i> gene (rs1004446_A), and non-HLA gene polymorphisms identified by the Type 1 Diabetes Genetics Consortium (T1DGC). 28903990 2017
dbSNP: rs1004446
rs1004446
Entrez Id: 3481;51214;723961
Gene Symbol: IGF2;IGF2-AS;INS-IGF2
IGF2;IGF2-AS;INS-IGF2
CUI: C0011854
Disease:
Diabetes Mellitus, Insulin-Dependent 		G 0.810 GeneticVariation GWASCAT Genome-wide association analysis of autoantibody positivity in type 1 diabetes cases. 21829393 2011
dbSNP: rs1004446
rs1004446
Entrez Id: 3481;51214;723961
Gene Symbol: IGF2;IGF2-AS;INS-IGF2
IGF2;IGF2-AS;INS-IGF2
CUI: C0011854
Disease:
Diabetes Mellitus, Insulin-Dependent 		C 0.810 GeneticVariation GWASDB A genome-wide association study identifies KIAA0350 as a type 1 diabetes gene. 17632545 2007
dbSNP: rs1004446
rs1004446
Entrez Id: 3481;51214;723961
Gene Symbol: IGF2;IGF2-AS;INS-IGF2
IGF2;IGF2-AS;INS-IGF2
CUI: C0011854
Disease:
Diabetes Mellitus, Insulin-Dependent 		C 0.810 GeneticVariation GWASCAT A genome-wide association study identifies KIAA0350 as a type 1 diabetes gene. 17632545 2007
dbSNP: rs3741208
rs3741208
Entrez Id: 3481;51214;723961
Gene Symbol: IGF2;IGF2-AS;INS-IGF2
IGF2;IGF2-AS;INS-IGF2
CUI: C0011854
Disease:
Diabetes Mellitus, Insulin-Dependent 		T 0.800 GeneticVariation GWASCAT Robust associations of four new chromosome regions from genome-wide analyses of type 1 diabetes. 17554260 2007
dbSNP: rs3741208
rs3741208
Entrez Id: 3481;51214;723961
Gene Symbol: IGF2;IGF2-AS;INS-IGF2
IGF2;IGF2-AS;INS-IGF2
CUI: C0011854
Disease:
Diabetes Mellitus, Insulin-Dependent 		T 0.800 GeneticVariation GWASDB Robust associations of four new chromosome regions from genome-wide analyses of type 1 diabetes. 17554260 2007
dbSNP: rs35506085
rs35506085
Entrez Id: 3481;51214;723961
Gene Symbol: IGF2;IGF2-AS;INS-IGF2
IGF2;IGF2-AS;INS-IGF2
CUI: C0005890
Disease:
Body Height 		0.700 GeneticVariation GWASCAT Leveraging Polygenic Functional Enrichment to Improve GWAS Power. 30595370 2019
dbSNP: rs35506085
rs35506085
Entrez Id: 3481;51214;723961
Gene Symbol: IGF2;IGF2-AS;INS-IGF2
IGF2;IGF2-AS;INS-IGF2
CUI: C0424678
Disease:
Lean body mass 		0.700 GeneticVariation GWASCAT Genomics of body fat percentage may contribute to sex bias in anorexia nervosa. 30593698 2019
dbSNP: rs35506085
rs35506085
Entrez Id: 3481;51214;723961
Gene Symbol: IGF2;IGF2-AS;INS-IGF2
IGF2;IGF2-AS;INS-IGF2
CUI: C0202239
Disease:
Uric acid measurement (procedure) 		A 0.700 GeneticVariation GWASCAT Target genes, variants, tissues and transcriptional pathways influencing human serum urate levels. 31578528 2019
dbSNP: rs3741205
rs3741205
Entrez Id: 3481;51214;723961
Gene Symbol: IGF2;IGF2-AS;INS-IGF2
IGF2;IGF2-AS;INS-IGF2
CUI: C0017654
Disease:
Glomerular Filtration Rate 		C 0.700 GeneticVariation GWASCAT Sex-specific and pleiotropic effects underlying kidney function identified from GWAS meta-analysis. 31015462 2019
dbSNP: rs3741210
rs3741210
Entrez Id: 3481;51214;723961
Gene Symbol: IGF2;IGF2-AS;INS-IGF2
IGF2;IGF2-AS;INS-IGF2
CUI: C0871470
Disease:
Systolic Pressure 		0.700 GeneticVariation GWASCAT Leveraging Polygenic Functional Enrichment to Improve GWAS Power. 30595370 2019
dbSNP: rs3741210
rs3741210
Entrez Id: 3481;51214;723961
Gene Symbol: IGF2;IGF2-AS;INS-IGF2
IGF2;IGF2-AS;INS-IGF2
CUI: C0202239
Disease:
Uric acid measurement (procedure) 		A 0.700 GeneticVariation GWASCAT Target genes, variants, tissues and transcriptional pathways influencing human serum urate levels. 31578528 2019
dbSNP: rs7948458
rs7948458
Entrez Id: 3481;723961
Gene Symbol: IGF2;INS-IGF2
IGF2;INS-IGF2
CUI: C0005910
Disease:
Body Weight 		0.700 GeneticVariation GWASCAT Multitrait genome association analysis identifies new susceptibility genes for human anthropometric variation in the GCAT cohort. 30166351 2018
dbSNP: rs149483638
rs149483638
Entrez Id: 3481;51214;723961
Gene Symbol: IGF2;IGF2-AS;INS-IGF2
IGF2;IGF2-AS;INS-IGF2
CUI: C0011860
Disease:
Diabetes Mellitus, Non-Insulin-Dependent 		C 0.700 GeneticVariation GWASCAT A Loss-of-Function Splice Acceptor Variant in IGF2 Is Protective for Type 2 Diabetes. 28838971 2017
dbSNP: rs17885785
rs17885785
Entrez Id: 3481;51214;723961
Gene Symbol: IGF2;IGF2-AS;INS-IGF2
IGF2;IGF2-AS;INS-IGF2
CUI: C3150797
Disease:
AUTOIMMUNE DISEASE, SUSCEPTIBILITY TO, 6 		T 0.700 GeneticVariation GWASCAT Meta-analysis of shared genetic architecture across ten pediatric autoimmune diseases. 26301688 2015
dbSNP: rs17885785
rs17885785
Entrez Id: 3481;51214;723961
Gene Symbol: IGF2;IGF2-AS;INS-IGF2
IGF2;IGF2-AS;INS-IGF2
CUI: C0010346
Disease:
Crohn Disease 		T 0.700 GeneticVariation GWASCAT Meta-analysis of shared genetic architecture across ten pediatric autoimmune diseases. 26301688 2015
dbSNP: rs17885785
rs17885785
Entrez Id: 3481;51214;723961
Gene Symbol: IGF2;IGF2-AS;INS-IGF2
IGF2;IGF2-AS;INS-IGF2
CUI: C0007570
Disease:
Celiac Disease 		T 0.700 GeneticVariation GWASCAT Meta-analysis of shared genetic architecture across ten pediatric autoimmune diseases. 26301688 2015
dbSNP: rs17885785
rs17885785
Entrez Id: 3481;51214;723961
Gene Symbol: IGF2;IGF2-AS;INS-IGF2
IGF2;IGF2-AS;INS-IGF2
CUI: C0038013
Disease:
Ankylosing spondylitis 		T 0.700 GeneticVariation GWASCAT Meta-analysis of shared genetic architecture across ten pediatric autoimmune diseases. 26301688 2015
dbSNP: rs17885785
rs17885785
Entrez Id: 3481;51214;723961
Gene Symbol: IGF2;IGF2-AS;INS-IGF2
IGF2;IGF2-AS;INS-IGF2
CUI: C0024141
Disease:
Lupus Erythematosus, Systemic 		T 0.700 GeneticVariation GWASCAT Meta-analysis of shared genetic architecture across ten pediatric autoimmune diseases. 26301688 2015
dbSNP: rs17885785
rs17885785
Entrez Id: 3481;51214;723961
Gene Symbol: IGF2;IGF2-AS;INS-IGF2
IGF2;IGF2-AS;INS-IGF2
CUI: C0920350
Disease:
Autoimmune thyroiditis 		T 0.700 GeneticVariation GWASCAT Meta-analysis of shared genetic architecture across ten pediatric autoimmune diseases. 26301688 2015
dbSNP: rs17885785
rs17885785
Entrez Id: 3481;51214;723961
Gene Symbol: IGF2;IGF2-AS;INS-IGF2
IGF2;IGF2-AS;INS-IGF2
CUI: C4014795
Disease:
AUTOIMMUNE DISEASE, MULTISYSTEM, INFANTILE-ONSET, 1 		T 0.700 GeneticVariation GWASCAT Meta-analysis of shared genetic architecture across ten pediatric autoimmune diseases. 26301688 2015
dbSNP: rs17885785
rs17885785
Entrez Id: 3481;51214;723961
Gene Symbol: IGF2;IGF2-AS;INS-IGF2
IGF2;IGF2-AS;INS-IGF2
CUI: C3495559
Disease:
Juvenile arthritis 		T 0.700 GeneticVariation GWASCAT Meta-analysis of shared genetic architecture across ten pediatric autoimmune diseases. 26301688 2015
dbSNP: rs17885785
rs17885785
Entrez Id: 3481;51214;723961
Gene Symbol: IGF2;IGF2-AS;INS-IGF2
IGF2;IGF2-AS;INS-IGF2
CUI: C0033860
Disease:
Psoriasis 		T 0.700 GeneticVariation GWASCAT Meta-analysis of shared genetic architecture across ten pediatric autoimmune diseases. 26301688 2015
dbSNP: rs17885785
rs17885785
Entrez Id: 3481;51214;723961
Gene Symbol: IGF2;IGF2-AS;INS-IGF2
IGF2;IGF2-AS;INS-IGF2
CUI: C0009447
Disease:
Common Variable Immunodeficiency 		T 0.700 GeneticVariation GWASCAT Meta-analysis of shared genetic architecture across ten pediatric autoimmune diseases. 26301688 2015
dbSNP: rs17885785
rs17885785
Entrez Id: 3481;51214;723961
Gene Symbol: IGF2;IGF2-AS;INS-IGF2
IGF2;IGF2-AS;INS-IGF2
CUI: C0011854
Disease:
Diabetes Mellitus, Insulin-Dependent 		T 0.700 GeneticVariation GWASCAT Meta-analysis of shared genetic architecture across ten pediatric autoimmune diseases. 26301688 2015