IGF2-AS, IGF2 antisense RNA, 51214

N. diseases: 65; N. variants: 10
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: C0011849
Disease:
Diabetes Mellitus
0.010 GeneticVariation BEFREE Three single nucleotide polymorphisms were associated with increased diabetes risk (rs10517086_A [<i>P</i> = 0.03], rs1534422_G [<i>P</i> = 0.006], and rs2327832_G [<i>P</i> = 0.03] in <i>TNFAIP3</i>) and one with decreased risk (rs1004446_A in <i>INS</i> [<i>P</i> = 0.006]). 28903990 2017
dbSNP: rs1004446
rs1004446
Entrez Id: 3481;51214;723961
Gene Symbol: IGF2;IGF2-AS;INS-IGF2
IGF2;IGF2-AS;INS-IGF2
CUI: C0011847
Disease:
Diabetes
0.010 GeneticVariation BEFREE Three single nucleotide polymorphisms were associated with increased diabetes risk (rs10517086_A [<i>P</i> = 0.03], rs1534422_G [<i>P</i> = 0.006], and rs2327832_G [<i>P</i> = 0.03] in <i>TNFAIP3</i>) and one with decreased risk (rs1004446_A in <i>INS</i> [<i>P</i> = 0.006]). 28903990 2017
dbSNP: rs10770125
rs10770125
Entrez Id: 3481;51214;723961
Gene Symbol: IGF2;IGF2-AS;INS-IGF2
IGF2;IGF2-AS;INS-IGF2
CUI: C0020456
Disease:
Hyperglycemia
0.010 GeneticVariation BEFREE Meta-analysis of the associations including data from 1367 Hyperglycaemia and Adverse Pregnancy Outcome Study participants confirmed the paternally-transmitted fetal IGF2/INS SNP associations (rs10770125, P-value=3.2×10<sup>-8</sup>, rs2585, P-value=3.6×10<sup>-5</sup>) and the composite fetal imprinted gene allele score association (P-value=1.3×10<sup>-8</sup>), but not the maternally-transmitted fetal KCNQ1(OT1) associations (rs231841, P-value=0.4; rs7929804, P-value=0.2). 28392167 2017
dbSNP: rs10770125
rs10770125
Entrez Id: 3481;51214;723961
Gene Symbol: IGF2;IGF2-AS;INS-IGF2
IGF2;IGF2-AS;INS-IGF2
CUI: C0085207
Disease:
Gestational Diabetes
0.010 GeneticVariation BEFREE Four fetal SNP alleles with the strongest univariate associations: paternally-transmitted IGF2 rs10770125 (P-value=2×10<sup>-4</sup>) and INS rs2585 (P-value=7×10<sup>-4</sup>), and maternally-transmitted KCNQ1(OT1) rs231841 (P-value=1×10<sup>-3</sup>) and KCNQ1(OT1) rs7929804 (P-value=4×10<sup>-3</sup>), were used to construct a composite fetal imprinted gene allele score which was associated with maternal glucose concentrations (P-value=4.3×10<sup>-6</sup>, n=981, r<sup>2</sup>=2.0%) and GDM prevalence (odds ratio per allele 1.44 (1.15, 1.80), P-value=1×10<sup>-3</sup>, n=89 cases and 899 controls). 28392167 2017
dbSNP: rs1003483
rs1003483
Entrez Id: 3481;51214;723961
Gene Symbol: IGF2;IGF2-AS;INS-IGF2
IGF2;IGF2-AS;INS-IGF2
CUI: C0271183
Disease:
Severe myopia
0.010 GeneticVariation BEFREE SNPs in the INS-IGF2 region (rs2070762 and rs1003483), and the INSR gene (rs3745551 and rs2229429) showed significant association with HM (allelic P = 0.0085, 0.0494, 0.0171 and 0.0238, respectively). 25266237 2015
dbSNP: rs10770125
rs10770125
Entrez Id: 3481;51214;723961
Gene Symbol: IGF2;IGF2-AS;INS-IGF2
IGF2;IGF2-AS;INS-IGF2
CUI: C0011881
Disease:
Diabetic Nephropathy
0.010 GeneticVariation BEFREE IGF2 rs10770125 was also associated with DN in male T1D patients of the GoKinD population (P=0.038, OR=0.67 95% CI 0.46-0.98). 22770937 2013
dbSNP: rs10770125
rs10770125
Entrez Id: 3481;51214;723961
Gene Symbol: IGF2;IGF2-AS;INS-IGF2
IGF2;IGF2-AS;INS-IGF2
CUI: C0011854
Disease:
Diabetes Mellitus, Insulin-Dependent
0.010 GeneticVariation BEFREE IGF2 rs10770125 was also associated with DN in male T1D patients of the GoKinD population (P=0.038, OR=0.67 95% CI 0.46-0.98). 22770937 2013
dbSNP: rs1004446
rs1004446
Entrez Id: 3481;51214;723961
Gene Symbol: IGF2;IGF2-AS;INS-IGF2
IGF2;IGF2-AS;INS-IGF2
CUI: C0007103
Disease:
Malignant neoplasm of endometrium
0.010 GeneticVariation BEFREE We observed an inverse association with IGFII rs3741211 and endometrial cancer risk (OR=0.79 (95% CI: 0.63, 0.99)) and IGFII rs1004446 and endometrial cancer risk (OR=0.80 (95% CI: 0.68, 0.94)). 21078522 2011
dbSNP: rs1004446
rs1004446
Entrez Id: 3481;51214;723961
Gene Symbol: IGF2;IGF2-AS;INS-IGF2
IGF2;IGF2-AS;INS-IGF2
CUI: C0476089
Disease:
Endometrial Carcinoma
0.010 GeneticVariation BEFREE We observed an inverse association with IGFII rs3741211 and endometrial cancer risk (OR=0.79 (95% CI: 0.63, 0.99)) and IGFII rs1004446 and endometrial cancer risk (OR=0.80 (95% CI: 0.68, 0.94)). 21078522 2011
dbSNP: rs3741211
rs3741211
Entrez Id: 3481;51214;723961
Gene Symbol: IGF2;IGF2-AS;INS-IGF2
IGF2;IGF2-AS;INS-IGF2
CUI: C0007103
Disease:
Malignant neoplasm of endometrium
0.010 GeneticVariation BEFREE We observed an inverse association with IGFII rs3741211 and endometrial cancer risk (OR=0.79 (95% CI: 0.63, 0.99)) and IGFII rs1004446 and endometrial cancer risk (OR=0.80 (95% CI: 0.68, 0.94)). 21078522 2011
dbSNP: rs3741211
rs3741211
Entrez Id: 3481;51214;723961
Gene Symbol: IGF2;IGF2-AS;INS-IGF2
IGF2;IGF2-AS;INS-IGF2
CUI: C0476089
Disease:
Endometrial Carcinoma
0.010 GeneticVariation BEFREE We observed an inverse association with IGFII rs3741211 and endometrial cancer risk (OR=0.79 (95% CI: 0.63, 0.99)) and IGFII rs1004446 and endometrial cancer risk (OR=0.80 (95% CI: 0.68, 0.94)). 21078522 2011
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: 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