OAS1, 2'-5'-oligoadenylate synthetase 1, 4938

N. diseases: 72; N. variants: 11
Source: ALL
Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs11066452
rs11066452
Entrez Id: 4938
Gene Symbol: OAS1
OAS1
CUI: C2985280
Disease:
Blood Protein Measurement
T 0.700 GeneticVariation GWASCAT Co-regulatory networks of human serum proteins link genetics to disease. 30072576 2018
dbSNP: rs4767027
rs4767027
Entrez Id: 4938
Gene Symbol: OAS1
OAS1
CUI: C2985280
Disease:
Blood Protein Measurement
C 0.700 GeneticVariation GWASCAT Genomic atlas of the human plasma proteome. 29875488 2018
dbSNP: rs10774671
rs10774671
Entrez Id: 4938
Gene Symbol: OAS1
OAS1
CUI: C0008055
Disease:
Chikungunya Fever
0.010 GeneticVariation BEFREE Polymorphisms in the promoter region of CD209 gene (rs735239, rs4804803, rs2287886) and OAS1 (rs1131454 and rs10774671), OAS2 (rs15895 and rs1732778), and OAS3 (rs2285932 and rs2072136) genes were investigated in 100 patients with CHIKV infection and 101 healthy controls to find out the association of these polymorphisms with CHIKV infection. 26398832 2016
dbSNP: rs1131454
rs1131454
Entrez Id: 4938
Gene Symbol: OAS1
OAS1
CUI: C0008055
Disease:
Chikungunya Fever
0.010 GeneticVariation BEFREE Polymorphisms in the promoter region of CD209 gene (rs735239, rs4804803, rs2287886) and OAS1 (rs1131454 and rs10774671), OAS2 (rs15895 and rs1732778), and OAS3 (rs2285932 and rs2072136) genes were investigated in 100 patients with CHIKV infection and 101 healthy controls to find out the association of these polymorphisms with CHIKV infection. 26398832 2016
dbSNP: rs10774671
rs10774671
Entrez Id: 4938
Gene Symbol: OAS1
OAS1
CUI: C0275524
Disease:
Coinfection
0.010 GeneticVariation BEFREE In this study, we examined the association between single-nucleotide polymorphisms (SNPs) in 3 innate immunity genes [2'-5'oligoadenylate synthetase 1 (OAS1) rs10774671, interleukin 28B (IL28B) rs12979860, and low molecular mass polypeptide 7 (LMP-7) at codon 49] besides cytomegalovirus (CMV) coinfection and susceptibility to HCC in genotype 4 (GT4) chronically infected Egyptian patients. 27726464 2016
dbSNP: rs10774671
rs10774671
Entrez Id: 4938
Gene Symbol: OAS1
OAS1
CUI: C0011311
Disease:
Dengue Fever
0.010 GeneticVariation BEFREE Polymorphisms in the OAS1 (rs1131454 and rs10774671), OAS3 (rs2285932 and rs2072136) and OAS2 (rs15895 and rs1732778) genes were studied using PCR followed by restriction fragment length polymorphism methods in 109 patients hospitalized for dengue (DEN) and 105 healthy controls (HCs) who have no documented evidence of symptomatic dengue. 23337612 2013
dbSNP: rs1131454
rs1131454
Entrez Id: 4938
Gene Symbol: OAS1
OAS1
CUI: C0011311
Disease:
Dengue Fever
0.010 GeneticVariation BEFREE Polymorphisms in the OAS1 (rs1131454 and rs10774671), OAS3 (rs2285932 and rs2072136) and OAS2 (rs15895 and rs1732778) genes were studied using PCR followed by restriction fragment length polymorphism methods in 109 patients hospitalized for dengue (DEN) and 105 healthy controls (HCs) who have no documented evidence of symptomatic dengue. 23337612 2013
dbSNP: rs10774671
rs10774671
Entrez Id: 4938
Gene Symbol: OAS1
OAS1
CUI: C0011854
Disease:
Diabetes Mellitus, Insulin-Dependent
0.030 GeneticVariation BEFREE Recently, it was reported that an A/G splice-site single nucleotide polymorphism (SNP; rs10774671) in the OAS1 gene, encoding 2'5'-oligoadenylate synthetase, was associated with a protective effect against type 1 diabetes in unaffected siblings, and yet affected siblings showed random transmission. 16644715 2006
dbSNP: rs10774671
rs10774671
Entrez Id: 4938
Gene Symbol: OAS1
OAS1
CUI: C0011854
Disease:
Diabetes Mellitus, Insulin-Dependent
0.030 GeneticVariation BEFREE We confirm the T1D association with rs10774671, but we conclude that it cannot be attributed (solely) to the splicing variant rs10774671. 16014697 2006
dbSNP: rs10774671
rs10774671
Entrez Id: 4938
Gene Symbol: OAS1
OAS1
CUI: C0011854
Disease:
Diabetes Mellitus, Insulin-Dependent
0.030 GeneticVariation BEFREE The data suggest that there may be a weak association with T1D for two OAS1 polymorphisms, rs3741981 and rs10774671, in populations of European descent. 19956105 2009
dbSNP: rs11066453
rs11066453
Entrez Id: 4938
Gene Symbol: OAS1
OAS1
CUI: C0011860
Disease:
Diabetes Mellitus, Non-Insulin-Dependent
G 0.800 GeneticVariation GWASDB New susceptibility loci in MYL2, C12orf51 and OAS1 associated with 1-h plasma glucose as predisposing risk factors for type 2 diabetes in the Korean population. 23575436 2013
dbSNP: rs11066453
rs11066453
Entrez Id: 4938
Gene Symbol: OAS1
OAS1
CUI: C0011860
Disease:
Diabetes Mellitus, Non-Insulin-Dependent
G 0.800 GeneticVariation GWASCAT New susceptibility loci in MYL2, C12orf51 and OAS1 associated with 1-h plasma glucose as predisposing risk factors for type 2 diabetes in the Korean population. 23575436 2013
dbSNP: rs10774671
rs10774671
Entrez Id: 4938
Gene Symbol: OAS1
OAS1
CUI: C0239946
Disease:
Fibrosis, Liver
0.010 GeneticVariation BEFREE Impact of OAS1 Exon 7 rs10774671 Genetic Variation on Liver Fibrosis Progression in Egyptian HCV Genotype 4 Patients. 26505957 2015
dbSNP: rs3741981
rs3741981
Entrez Id: 4938
Gene Symbol: OAS1
OAS1
CUI: C0239946
Disease:
Fibrosis, Liver
0.010 GeneticVariation BEFREE The polymorphism at OAS1 exon 7 rs3741981 might be a potential genetic marker and can be useful in the assessment of liver fibrosis progression and disease outcome in HCV-infected patients. 26505957 2015
dbSNP: rs11066453
rs11066453
Entrez Id: 4938
Gene Symbol: OAS1
OAS1
CUI: C0202035
Disease:
Gamma glutamyl transferase measurement
G 0.700 GeneticVariation GWASDB Large-scale genome-wide association studies in East Asians identify new genetic loci influencing metabolic traits. 21909109 2011
dbSNP: rs10774671
rs10774671
Entrez Id: 4938
Gene Symbol: OAS1
OAS1
CUI: C0018572
Disease:
Hand, Foot and Mouth Disease
0.010 GeneticVariation BEFREE In short, the OAS1 rs10774671 SNP GG genotype contributed to CA16 susceptibility and was associated with the development of mild HFMD. 25059424 2014
dbSNP: rs10774671
rs10774671
Entrez Id: 4938
Gene Symbol: OAS1
OAS1
CUI: C0019163
Disease:
Hepatitis B
0.010 GeneticVariation BEFREE Our data demonstrated that the functional variant, rs10774671, is associated with HBV infection and anti-SSA antibody-positive SS. 29242559 2017
dbSNP: rs10774671
rs10774671
Entrez Id: 4938
Gene Symbol: OAS1
OAS1
CUI: C0019196
Disease:
Hepatitis C
0.020 GeneticVariation BEFREE Impact of OAS1 Exon 7 rs10774671 Genetic Variation on Liver Fibrosis Progression in Egyptian HCV Genotype 4 Patients. 26505957 2015
dbSNP: rs10774671
rs10774671
Entrez Id: 4938
Gene Symbol: OAS1
OAS1
CUI: C0019196
Disease:
Hepatitis C
0.020 GeneticVariation BEFREE Moreover, individuals carrying the A allele in these SNPs exhibited an increased risk for chronic HCV infection (rs2660 and rs10774671</span>: OR = 1.356 [1.051-1.749]; rs3741981: 1.363 [1.085-1.712]). 22710942 2013
dbSNP: rs3741981
rs3741981
Entrez Id: 4938
Gene Symbol: OAS1
OAS1
CUI: C0019196
Disease:
Hepatitis C
0.020 GeneticVariation BEFREE The polymorphism at OAS1 exon 7 rs3741981 might be a potential genetic marker and can be useful in the assessment of liver fibrosis progression and disease outcome in HCV-infected patients. 26505957 2015
dbSNP: rs3741981
rs3741981
Entrez Id: 4938
Gene Symbol: OAS1
OAS1
CUI: C0019196
Disease:
Hepatitis C
0.020 GeneticVariation BEFREE Moreover, individuals carrying the A allele in these SNPs exhibited an increased risk for chronic HCV infection (rs2660 and rs10774671: OR = 1.356 [1.051-1.749]; rs3741981: 1.363 [1.085-1.712]). 22710942 2013
dbSNP: rs2660
rs2660
Entrez Id: 4938
Gene Symbol: OAS1
OAS1
CUI: C0019196
Disease:
Hepatitis C
0.010 GeneticVariation BEFREE Moreover, individuals carrying the A allele in these SNPs exhibited an increased risk for chronic HCV infection (rs2660 and rs10774671: OR = 1.356 [1.051-1.749]; rs3741981: 1.363 [1.085-1.712]). 22710942 2013
dbSNP: rs10774671
rs10774671
Entrez Id: 4938
Gene Symbol: OAS1
OAS1
CUI: C2239176
Disease:
Liver carcinoma
0.010 GeneticVariation BEFREE However, OAS1 rs10774671 does not seem to contribute to the development of HCC. 27726464 2016
dbSNP: rs4766676
rs4766676
Entrez Id: 4938
Gene Symbol: OAS1
OAS1
CUI: C0200635
Disease:
Lymphocyte Count measurement
0.700 GeneticVariation GWASDB The combination of a genome-wide association study of lymphocyte count and analysis of gene expression data reveals novel asthma candidate genes. 22286170 2012
dbSNP: rs2660
rs2660
Entrez Id: 4938
Gene Symbol: OAS1
OAS1
CUI: C0376358
Disease:
Malignant neoplasm of prostate
0.010 GeneticVariation BEFREE OAS1 rs2660 may be a prostate cancer susceptibility polymorphism, which is a significant observation, especially in a context of the OAS1-RNaseL pathway. 21638280 2011