Source: GWASCAT

Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs1004446
rs1004446
IGF2 ; IGF2-AS ; INS-IGF2
CUI: C0011854
Disease: Diabetes Mellitus, Insulin-Dependent
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
IGF2 ; IGF2-AS ; INS-IGF2
CUI: C0011854
Disease: Diabetes Mellitus, Insulin-Dependent
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
IGF2 ; IGF2-AS ; INS-IGF2
CUI: C0011854
Disease: Diabetes Mellitus, Insulin-Dependent
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: rs149483638
rs149483638
IGF2 ; IGF2-AS ; INS-IGF2
CUI: C0011860
Disease: Diabetes Mellitus, Non-Insulin-Dependent
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
IGF2 ; IGF2-AS ; INS-IGF2
CUI: C0920350
Disease: Autoimmune thyroiditis
Autoimmune thyroiditis 		T 0.700 GeneticVariation GWASCAT Meta-analysis of shared genetic architecture across ten pediatric autoimmune diseases. 26301688

2015
dbSNP: rs17885785
rs17885785
IGF2 ; IGF2-AS ; INS-IGF2
CUI: C0009447
Disease: Common Variable Immunodeficiency
Common Variable Immunodeficiency 		T 0.700 GeneticVariation GWASCAT Meta-analysis of shared genetic architecture across ten pediatric autoimmune diseases. 26301688

2015
dbSNP: rs17885785
rs17885785
IGF2 ; IGF2-AS ; INS-IGF2
CUI: C3495559
Disease: Juvenile arthritis
Juvenile arthritis 		T 0.700 GeneticVariation GWASCAT Meta-analysis of shared genetic architecture across ten pediatric autoimmune diseases. 26301688

2015
dbSNP: rs17885785
rs17885785
IGF2 ; IGF2-AS ; INS-IGF2
CUI: C0033860
Disease: Psoriasis
Psoriasis 		T 0.700 GeneticVariation GWASCAT Meta-analysis of shared genetic architecture across ten pediatric autoimmune diseases. 26301688

2015
dbSNP: rs17885785
rs17885785
IGF2 ; IGF2-AS ; INS-IGF2
CUI: C0011854
Disease: Diabetes Mellitus, Insulin-Dependent
Diabetes Mellitus, Insulin-Dependent 		T 0.700 GeneticVariation GWASCAT Meta-analysis of shared genetic architecture across ten pediatric autoimmune diseases. 26301688

2015
dbSNP: rs17885785
rs17885785
IGF2 ; IGF2-AS ; INS-IGF2
CUI: C0038013
Disease: Ankylosing spondylitis
Ankylosing spondylitis 		T 0.700 GeneticVariation GWASCAT Meta-analysis of shared genetic architecture across ten pediatric autoimmune diseases. 26301688

2015
dbSNP: rs17885785
rs17885785
IGF2 ; IGF2-AS ; INS-IGF2
CUI: C0010346
Disease: Crohn Disease
Crohn Disease 		T 0.700 GeneticVariation GWASCAT Meta-analysis of shared genetic architecture across ten pediatric autoimmune diseases. 26301688

2015
dbSNP: rs17885785
rs17885785
IGF2 ; IGF2-AS ; INS-IGF2
CUI: C3150797
Disease: AUTOIMMUNE DISEASE, SUSCEPTIBILITY TO, 6
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
IGF2 ; IGF2-AS ; INS-IGF2
CUI: C0007570
Disease: Celiac Disease
Celiac Disease 		T 0.700 GeneticVariation GWASCAT Meta-analysis of shared genetic architecture across ten pediatric autoimmune diseases. 26301688

2015
dbSNP: rs17885785
rs17885785
IGF2 ; IGF2-AS ; INS-IGF2
CUI: C0004364
Disease: Autoimmune Diseases
Autoimmune Diseases 		T 0.700 GeneticVariation GWASCAT Meta-analysis of shared genetic architecture across ten pediatric autoimmune diseases. 26301688

2015
dbSNP: rs17885785
rs17885785
IGF2 ; IGF2-AS ; INS-IGF2
CUI: C0024141
Disease: Lupus Erythematosus, Systemic
Lupus Erythematosus, Systemic 		T 0.700 GeneticVariation GWASCAT Meta-analysis of shared genetic architecture across ten pediatric autoimmune diseases. 26301688

2015
dbSNP: rs17885785
rs17885785
IGF2 ; IGF2-AS ; INS-IGF2
CUI: C0009324
Disease: Ulcerative Colitis
Ulcerative Colitis 		T 0.700 GeneticVariation GWASCAT Meta-analysis of shared genetic architecture across ten pediatric autoimmune diseases. 26301688

2015
dbSNP: rs17885785
rs17885785
IGF2 ; IGF2-AS ; INS-IGF2
CUI: C4014795
Disease: AUTOIMMUNE DISEASE, MULTISYSTEM, INFANTILE-ONSET, 1
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
IGF2 ; IGF2-AS ; INS-IGF2
CUI: C4310768
Disease: AUTOIMMUNE DISEASE, MULTISYSTEM, INFANTILE-ONSET, 2
AUTOIMMUNE DISEASE, MULTISYSTEM, INFANTILE-ONSET, 2 		T 0.700 GeneticVariation GWASCAT Meta-analysis of shared genetic architecture across ten pediatric autoimmune diseases. 26301688

2015
dbSNP: rs35506085
rs35506085
IGF2 ; IGF2-AS ; INS-IGF2
CUI: C0424678
Disease: Lean body mass
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
IGF2 ; IGF2-AS ; INS-IGF2
CUI: C0005890
Disease: Body Height
Body Height 		0.700 GeneticVariation GWASCAT Leveraging Polygenic Functional Enrichment to Improve GWAS Power. 30595370

2019
dbSNP: rs35506085
rs35506085
IGF2 ; IGF2-AS ; INS-IGF2
CUI: C0202239
Disease: Uric acid measurement (procedure)
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
IGF2 ; IGF2-AS ; INS-IGF2
CUI: C0017654
Disease: Glomerular Filtration Rate
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
IGF2 ; IGF2-AS ; INS-IGF2
CUI: C0202239
Disease: Uric acid measurement (procedure)
Uric acid measurement (procedure) 		A 0.700 GeneticVariation GWASCAT Target genes, variants, tissues and transcriptional pathways influencing human serum urate levels. 31578528

2019
dbSNP: rs3741210
rs3741210
IGF2 ; IGF2-AS ; INS-IGF2
CUI: C0871470
Disease: Systolic Pressure
Systolic Pressure 		0.700 GeneticVariation GWASCAT Leveraging Polygenic Functional Enrichment to Improve GWAS Power. 30595370

2019
dbSNP: rs7948458
rs7948458
IGF2 ; INS-IGF2
CUI: C0005910
Disease: Body Weight
Body Weight 		0.700 GeneticVariation GWASCAT Multitrait genome association analysis identifies new susceptibility genes for human anthropometric variation in the GCAT cohort. 30166351

2018