SNP Detail For rs11121451
1.Mapping Information
Human SNP ID rs11121451
Human chromosome chr1
Human SNP position 9613785
Pig chromosome chr6
Pig SNP position 64120238
2.Annotation Information
PubMed ID25839716
JournalEnviron Res
Linkwww.ncbi.nlm.nih.gov/pubmed/25839716
StudyGenome-wide association study of plasma levels of polychlorinated biphenyls disclose an association with the CYP2B6 gene in a population-based sample.
Disease/TraitPolychlorinated biphenyl levels
Initial sample922 European ancestry individuals
Replication sampleNA
Region1p36.22
Chromosome idchr1
Chromosome position9613785
Reported geneNR
Mapped geneTMEM201
Upstream gene id
Downstream gene id
SNP gene ids199953
Upstream gene distance
Downstream gene distance
SNP risk allelers11121451-?
SNPsrs11121451
Merged0
SNP id current11121451
Context3_prime_UTR_variant
Intergenic0
Allele frequency
P value0.0000003
Pvalue mlog6.52287874528033
P value text(PCB170)
Or beta1.55
%95 Ci[0.96-2.14] unit decrease
PlatformIllumina [8736858] (imputed)
CNVN
Mapped traitpolychlorinated biphenyls measurement
Mapped trait URIhttp://www.ebi.ac.uk/efo/EFO_0007042
Study accessionGCST002839
PubMed ID25839716
JournalEnviron Res
Linkwww.ncbi.nlm.nih.gov/pubmed/25839716
StudyGenome-wide association study of plasma levels of polychlorinated biphenyls disclose an association with the CYP2B6 gene in a population-based sample.
Disease/TraitPolychlorinated biphenyl levels
Initial sample922 European ancestry individuals
Replication sampleNA
Region1p36.22
Chromosome idchr1
Chromosome position9613785
Reported geneNR
Mapped geneTMEM201
Upstream gene id
Downstream gene id
SNP gene ids199953
Upstream gene distance
Downstream gene distance
SNP risk allelers11121451-?
SNPsrs11121451
Merged0
SNP id current11121451
Context3_prime_UTR_variant
Intergenic0
Allele frequency
P value0.0000001
Pvalue mlog7
P value text(PCB180)
Or beta1.66
%95 Ci[1.05-2.27] unit decrease
PlatformIllumina [8736858] (imputed)
CNVN
Mapped traitpolychlorinated biphenyls measurement
Mapped trait URIhttp://www.ebi.ac.uk/efo/EFO_0007042
Study accessionGCST002839