PTGS1, prostaglandin-endoperoxide synthase 1, 5742

N. diseases: 318; N. variants: 36
Source: ALL
Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs10306114
rs10306114
Entrez Id: 5742
Gene Symbol: PTGS1
PTGS1
CUI: C0595921
Disease:
Intraocular pressure disorder
0.010 GeneticVariation BEFREE Multiple regression analysis showed that heterozygous genotypes of rs10306114, rs11568658, and carrier of AT haplotype were significantly correlated with the lower %ΔIOP. 25339146 2015
dbSNP: rs10306121
rs10306121
Entrez Id: 5742
Gene Symbol: PTGS1
PTGS1
CUI: C0428474
Disease:
Serum LDL cholesterol measurement
0.700 GeneticVariation GWASDB Large-scale gene-centric meta-analysis across 32 studies identifies multiple lipid loci. 23063622 2012
dbSNP: rs10306121
rs10306121
Entrez Id: 5742
Gene Symbol: PTGS1
PTGS1
CUI: C0202117
Disease:
Low density lipoprotein cholesterol measurement
0.700 GeneticVariation GWASDB Large-scale gene-centric meta-analysis across 32 studies identifies multiple lipid loci. 23063622 2012
dbSNP: rs10306135
rs10306135
Entrez Id: 5742
Gene Symbol: PTGS1
PTGS1
CUI: C0007222
Disease:
Cardiovascular Diseases
0.010 GeneticVariation BEFREE Furthermore, individuals homozygote for the variant allele rs10306135 had lower prevalence of CVD, compared to the common allele (0% versus 30%, P=0.0047). 19091535 2009
dbSNP: rs10306137
rs10306137
Entrez Id: 5742
Gene Symbol: PTGS1
PTGS1
CUI: C0428474
Disease:
Serum LDL cholesterol measurement
0.700 GeneticVariation GWASDB Large-scale gene-centric meta-analysis across 32 studies identifies multiple lipid loci. 23063622 2012
dbSNP: rs10306137
rs10306137
Entrez Id: 5742
Gene Symbol: PTGS1
PTGS1
CUI: C1445957
Disease:
Serum total cholesterol measurement
0.700 GeneticVariation GWASDB Large-scale gene-centric meta-analysis across 32 studies identifies multiple lipid loci. 23063622 2012
dbSNP: rs10306137
rs10306137
Entrez Id: 5742
Gene Symbol: PTGS1
PTGS1
CUI: C0202117
Disease:
Low density lipoprotein cholesterol measurement
0.700 GeneticVariation GWASDB Large-scale gene-centric meta-analysis across 32 studies identifies multiple lipid loci. 23063622 2012
dbSNP: rs10306141
rs10306141
Entrez Id: 5742
Gene Symbol: PTGS1
PTGS1
CUI: C0023467
Disease:
Leukemia, Myelocytic, Acute
C 0.700 GeneticVariation GWASCAT Genome-wide haplotype association study identify the FGFR2 gene as a risk gene for acute myeloid leukemia. 27903959 2017
dbSNP: rs10306152
rs10306152
Entrez Id: 5742
Gene Symbol: PTGS1
PTGS1
CUI: C0023467
Disease:
Leukemia, Myelocytic, Acute
C 0.700 GeneticVariation GWASCAT Genome-wide haplotype association study identify the FGFR2 gene as a risk gene for acute myeloid leukemia. 27903959 2017
dbSNP: rs10306156
rs10306156
Entrez Id: 5742
Gene Symbol: PTGS1
PTGS1
CUI: C0023467
Disease:
Leukemia, Myelocytic, Acute
T 0.700 GeneticVariation GWASCAT Genome-wide haplotype association study identify the FGFR2 gene as a risk gene for acute myeloid leukemia. 27903959 2017
dbSNP: rs10306157
rs10306157
Entrez Id: 5742
Gene Symbol: PTGS1
PTGS1
CUI: C0023467
Disease:
Leukemia, Myelocytic, Acute
G 0.700 GeneticVariation GWASCAT Genome-wide haplotype association study identify the FGFR2 gene as a risk gene for acute myeloid leukemia. 27903959 2017
dbSNP: rs10306166
rs10306166
Entrez Id: 5742
Gene Symbol: PTGS1
PTGS1
CUI: C0023467
Disease:
Leukemia, Myelocytic, Acute
G 0.700 GeneticVariation GWASCAT Genome-wide haplotype association study identify the FGFR2 gene as a risk gene for acute myeloid leukemia. 27903959 2017
dbSNP: rs10306182
rs10306182
Entrez Id: 5742
Gene Symbol: PTGS1
PTGS1
CUI: C0023467
Disease:
Leukemia, Myelocytic, Acute
T 0.700 GeneticVariation GWASCAT Genome-wide haplotype association study identify the FGFR2 gene as a risk gene for acute myeloid leukemia. 27903959 2017
dbSNP: rs10306183
rs10306183
Entrez Id: 5742
Gene Symbol: PTGS1
PTGS1
CUI: C0023467
Disease:
Leukemia, Myelocytic, Acute
C 0.700 GeneticVariation GWASCAT Genome-wide haplotype association study identify the FGFR2 gene as a risk gene for acute myeloid leukemia. 27903959 2017
dbSNP: rs10306184
rs10306184
Entrez Id: 5742
Gene Symbol: PTGS1
PTGS1
CUI: C0023467
Disease:
Leukemia, Myelocytic, Acute
T 0.700 GeneticVariation GWASCAT Genome-wide haplotype association study identify the FGFR2 gene as a risk gene for acute myeloid leukemia. 27903959 2017
dbSNP: rs10306194
rs10306194
Entrez Id: 5742
Gene Symbol: PTGS1
PTGS1
CUI: C0023467
Disease:
Leukemia, Myelocytic, Acute
C 0.700 GeneticVariation GWASCAT Genome-wide haplotype association study identify the FGFR2 gene as a risk gene for acute myeloid leukemia. 27903959 2017
dbSNP: rs1160235906
rs1160235906
Entrez Id: 5742
Gene Symbol: PTGS1
PTGS1
CUI: C0578870
Disease:
Chronic idiopathic urticaria
0.010 GeneticVariation BEFREE A multiple regression model was found to show that COX-2 5'UTR T/G, COX-2 Exon 10 T/C, and FLAP -336 G/A polymorphisms were significantly associated with CSU, with the minor allele more represented in CSU group. 21227888 2011
dbSNP: rs1213266
rs1213266
Entrez Id: 5742
Gene Symbol: PTGS1
PTGS1
CUI: C0009402
Disease:
Colorectal Carcinoma
0.010 GeneticVariation BEFREE One, G>A intron 9 (rs1213266), was associated with approximately 50% lower CRC mortality (HR(AA/AG vs. GG) = 0.48; 95% CI, 0.25-0.93). 21976545 2011
dbSNP: rs1216603398
rs1216603398
Entrez Id: 5742
Gene Symbol: PTGS1
PTGS1
CUI: C0009402
Disease:
Colorectal Carcinoma
0.010 GeneticVariation BEFREE On the contrary, two other SNPs, PLA2G2A c.435+230C>T and PPARG c.1431C>T (p.His477His), were associated with a decrease in CRC risk. 18992148 2008
dbSNP: rs1256318228
rs1256318228
Entrez Id: 5742
Gene Symbol: PTGS1
PTGS1
CUI: C0013395
Disease:
Dyspepsia
0.010 GeneticVariation BEFREE On the other hand, the association between T allele of GNB3 C825T polymorphism and dyspepsia was reported from Japan and Netherlands. 21443717 2011
dbSNP: rs1300938986
rs1300938986
Entrez Id: 5742
Gene Symbol: PTGS1
PTGS1
CUI: C1561643
Disease:
Chronic Kidney Diseases
0.010 GeneticVariation BEFREE Subsequent multivariable logistic regression analysis with adjustment for covariates as well as a stepwise forward selection procedure revealed that the T --> C (Val591Ala) polymorphism of APOB (rs679899), the -681C --> G polymorphism of PPARG (rs10865710), the T --> C (Cys1367Arg) polymorphism of WRN (rs1346044), the -850C --> T polymorphism of TNF (rs1799724), the -219G --> T polymorphism of APOE (rs405509), the C --> T polymorphism of PTGS1 (rs883484) and the 41A --> G (Glu14Gly) polymorphism of ACAT2 (rs9658625) were significantly (P<0.05) associated with the prevalence of CKD. 19282863 2009
dbSNP: rs1330344
rs1330344
Entrez Id: 5742
Gene Symbol: PTGS1
PTGS1
CUI: C0948008
Disease:
Ischemic stroke
0.020 GeneticVariation BEFREE In conclusion, in Chinese patients with ischemic stroke and treated with aspirin, CC genotype of rs1330344 may increase the risk of subsequent vascular events. 24930730 2014
dbSNP: rs1330344
rs1330344
Entrez Id: 5742
Gene Symbol: PTGS1
PTGS1
CUI: C0948008
Disease:
Ischemic stroke
0.020 GeneticVariation BEFREE At rs1330344</span>, AA genotype may reduce the susceptibility of ischemic stroke. 31735164 2019
dbSNP: rs1330344
rs1330344
Entrez Id: 5742
Gene Symbol: PTGS1
PTGS1
CUI: C0850666
Disease:
Infection caused by Helicobacter pylori
0.010 GeneticVariation BEFREE Using the Chi-square test and logistic regression, we found that peptic ulcer history (odds ratio [OR] = 5.924, 95% confidence intervals [CI]: 2.115-16.592), dual anti-platelet medication (OR = 3.443, 95% CI: 1.154-10.271), current Helicobacter pylori infection (OR = 2.242, 95% CI: 1.032-4.870), male gender (OR = 2.211, 95% CI: 1.027-4.760), GG genotype of rs2243086 (OR = 4.516, 95% CI: 1.180-17.278), and AA genotype of rs1330344 (OR = 2.178, 95% CI: 1.016-4.669) were more frequent in subgroup A than subgroup B. 26830988 2016
dbSNP: rs1378013115
rs1378013115
Entrez Id: 5742
Gene Symbol: PTGS1
PTGS1
CUI: C0948008
Disease:
Ischemic stroke
0.010 GeneticVariation BEFREE To investigate whether single nucleotide polymorphisms (SNPs) of eicosanoid biosynthesis genes are associated with intracerebral hemorrhage (ICH) and ischemic stroke (IS), seven SNPs in the coding or promoter regions were selected: ALOX12 (rs434473, Asn322Ser), ALOX5 (rs2228064, Thr90Thr), ALOX5AP (rs17222919, -1316T/G), PTGES (rs7872802, -404A/G), PTGIS (rs5628, Leu256Leu), PTGS1 (rs3842788, Gln41Gln) and PTGS2 (rs5275, 3'UTR). 21816595 2011