SNP Detail For rs1495741
1.Mapping Information
Human SNP ID rs1495741
Human chromosome chr8
Human SNP position 18415371
Pig chromosome chr17
Pig SNP position 14143777
2.Annotation Information
PubMed ID20686565
JournalNature
Linkwww.ncbi.nlm.nih.gov/pubmed/20686565
StudyBiological, clinical and population relevance of 95 loci for blood lipids.
Disease/TraitTriglycerides
Initial sample96,598 European ancestry individuals
Replication sampleNA
Region8p22
Chromosome idchr8
Chromosome position18415371
Reported geneNAT2
Mapped geneNAT2 - PSD3
Upstream gene id10
Downstream gene id23362
SNP gene ids
Upstream gene distance14152
Downstream gene distance111932
SNP risk allelers1495741-G
SNPsrs1495741
Merged0
SNP id current1495741
Contextintergenic_variant
Intergenic1
Allele frequency0.22
P value0.00000000000004
Pvalue mlog13.397940008672
P value text
Or beta2.97
%95 Ci[2.15-3.79] mg/dL increase
PlatformAffymetrix, Illumina, Perlegen [~ 2600000] (imputed)
CNVN
Mapped traittriglyceride measurement
Mapped trait URIhttp://www.ebi.ac.uk/efo/EFO_0004530
Study accessionGCST000758
PubMed ID20972438
JournalNat Genet
Linkwww.ncbi.nlm.nih.gov/pubmed/20972438
StudyA multi-stage genome-wide association study of bladder cancer identifies multiple susceptibility loci.
Disease/TraitBladder cancer
Initial sample3,532 European ancestry cases, 5,120 European ancestry controls
Replication sample8,381 cases, 48,275 controls
Region8p22
Chromosome idchr8
Chromosome position18415371
Reported geneNAT2
Mapped geneNAT2 - PSD3
Upstream gene id10
Downstream gene id23362
SNP gene ids
Upstream gene distance14152
Downstream gene distance111932
SNP risk allelers1495741-?
SNPsrs1495741
Merged0
SNP id current1495741
Contextintergenic_variant
Intergenic1
Allele frequency0.8
P value0.00000000004
Pvalue mlog10.397940008672
P value text
Or beta1.15
%95 Ci[1.10-1.20]
PlatformIllumina [589299]
CNVN
Mapped traitbladder carcinoma
Mapped trait URIhttp://www.ebi.ac.uk/efo/EFO_0000292
Study accessionGCST000842
PubMed ID20686565
JournalNature
Linkwww.ncbi.nlm.nih.gov/pubmed/20686565
StudyBiological, clinical and population relevance of 95 loci for blood lipids.
Disease/TraitCholesterol, total
Initial sample100,184 European ancestry individuals
Replication sampleNA
Region8p22
Chromosome idchr8
Chromosome position18415371
Reported geneNAT2
Mapped geneNAT2 - PSD3
Upstream gene id10
Downstream gene id23362
SNP gene ids
Upstream gene distance14152
Downstream gene distance111932
SNP risk allelers1495741-G
SNPsrs1495741
Merged0
SNP id current1495741
Contextintergenic_variant
Intergenic1
Allele frequency0.32
P value0.000000002
Pvalue mlog8.69897000433601
P value text
Or beta1.07
%95 Ci[0.66-1.48] mg/dL increase
PlatformAffymetrix, Illumina, Perlegen [~ 2600000] (imputed)
CNVN
Mapped traittotal cholesterol measurement
Mapped trait URIhttp://www.ebi.ac.uk/efo/EFO_0004574
Study accessionGCST000760
PubMed ID24163127
JournalHum Mol Genet
Linkwww.ncbi.nlm.nih.gov/pubmed/24163127
StudyGenome-wide association study identifies multiple loci associated with bladder cancer risk.
Disease/TraitBladder cancer
Initial sampleup to 2,305 European ancestry cases, up to 3,901 European ancestry controls
Replication sampleup to 13,298 cases, up to 54,535 controls
Region8p22
Chromosome idchr8
Chromosome position18415371
Reported geneNAT2
Mapped geneNAT2 - PSD3
Upstream gene id10
Downstream gene id23362
SNP gene ids
Upstream gene distance14152
Downstream gene distance111932
SNP risk allelers1495741-A
SNPsrs1495741
Merged0
SNP id current1495741
Contextintergenic_variant
Intergenic1
Allele frequency0.8
P value0.0000000002
Pvalue mlog9.69897000433601
P value text
Or beta1.14
%95 Ci[1.09-1.18]
PlatformIllumina [462190]
CNVN
Mapped traitbladder carcinoma
Mapped trait URIhttp://www.ebi.ac.uk/efo/EFO_0000292
Study accessionGCST002240
PubMed ID24816252
JournalNat Genet
Linkwww.ncbi.nlm.nih.gov/pubmed/24816252
StudyAn atlas of genetic influences on human blood metabolites.
Disease/TraitBlood metabolite levels
Initial sample7,824 European ancestry individuals
Replication sampleNA
Region8p22
Chromosome idchr8
Chromosome position18415371
Reported geneNAT2
Mapped geneNAT2 - PSD3
Upstream gene id10
Downstream gene id23362
SNP gene ids
Upstream gene distance14152
Downstream gene distance111932
SNP risk allelers1495741-A
SNPsrs1495741
Merged0
SNP id current1495741
Contextintergenic_variant
Intergenic1
Allele frequency0.78
P value1E-27
Pvalue mlog27
P value text(1-methylurate)
Or beta0.057
%95 Ci[0.047-0.067] unit increase
PlatformAffymetrix, Illumina [2100000] (imputed)
CNVN
Mapped traitblood metabolite measurement
Mapped trait URIhttp://www.ebi.ac.uk/efo/EFO_0005664
Study accessionGCST002443
PubMed ID24097068
JournalNat Genet
Linkwww.ncbi.nlm.nih.gov/pubmed/24097068
StudyDiscovery and refinement of loci associated with lipid levels.
Disease/TraitCholesterol, total
Initial sample94,595 European ancestry individuals
Replication sample93,982 European ancestry individuals
Region8p22
Chromosome idchr8
Chromosome position18415371
Reported geneNAT2
Mapped geneNAT2 - PSD3
Upstream gene id10
Downstream gene id23362
SNP gene ids
Upstream gene distance14152
Downstream gene distance111932
SNP risk allelers1495741-G
SNPsrs1495741
Merged0
SNP id current1495741
Contextintergenic_variant
Intergenic1
Allele frequency0.26
P value0.00000003
Pvalue mlog7.52287874528033
P value text
Or beta0.032
%95 Ci[NR] unit increase
PlatformNR [NR] (imputed)
CNVN
Mapped traittotal cholesterol measurement
Mapped trait URIhttp://www.ebi.ac.uk/efo/EFO_0004574
Study accessionGCST002221
PubMed ID24097068
JournalNat Genet
Linkwww.ncbi.nlm.nih.gov/pubmed/24097068
StudyDiscovery and refinement of loci associated with lipid levels.
Disease/TraitTriglycerides
Initial sample94,595 European ancestry individuals
Replication sample93,982 European ancestry individuals
Region8p22
Chromosome idchr8
Chromosome position18415371
Reported geneNAT2
Mapped geneNAT2 - PSD3
Upstream gene id10
Downstream gene id23362
SNP gene ids
Upstream gene distance14152
Downstream gene distance111932
SNP risk allelers1495741-G
SNPsrs1495741
Merged0
SNP id current1495741
Contextintergenic_variant
Intergenic1
Allele frequency0.26
P value0.000000000003
Pvalue mlog11.5228787452803
P value text
Or beta0.04
%95 Ci[NR] mg/dL increase
PlatformNR [NR] (imputed)
CNVN
Mapped traittriglyceride measurement
Mapped trait URIhttp://www.ebi.ac.uk/efo/EFO_0004530
Study accessionGCST002216