SNP Detail For rs11067763
1.Mapping Information
Human SNP ID rs11067763
Human chromosome chr12
Human SNP position 115760536
Pig chromosome chr14
Pig SNP position 38857800
2.Annotation Information
PubMed ID25249183
JournalHum Mol Genet
Linkwww.ncbi.nlm.nih.gov/pubmed/25249183
StudyGenome-wide association study in Chinese identifies novel loci for blood pressure and hypertension.
Disease/TraitSystolic blood pressure
Initial sample11,816 Han Chinese ancestry individuals
Replication sample69,146 Han Chinese ancestry individuals
Region12q24.21
Chromosome idchr12
Chromosome position115760536
Reported geneMED13L
Mapped geneLOC105370003
Upstream gene id
Downstream gene id
SNP gene ids105370003
Upstream gene distance
Downstream gene distance
SNP risk allelers11067763-A
SNPsrs11067763
Merged0
SNP id current11067763
Contextintron_variant
Intergenic0
Allele frequency0.62
P value0.0000000000000006
Pvalue mlog15.2218487496163
P value text
Or beta0.81
%95 Ci[0.61-1.01] unit increase
PlatformAffymetrix, Illumina [2485448] (imputed)
CNVN
Mapped traitsystolic blood pressure
Mapped trait URIhttp://www.ebi.ac.uk/efo/EFO_0006335
Study accessionGCST002630
PubMed ID25249183
JournalHum Mol Genet
Linkwww.ncbi.nlm.nih.gov/pubmed/25249183
StudyGenome-wide association study in Chinese identifies novel loci for blood pressure and hypertension.
Disease/TraitDiastolic blood pressure
Initial sample11,816 Han Chinese ancestry individuals
Replication sample69,146 Han Chinese ancestry individuals
Region12q24.21
Chromosome idchr12
Chromosome position115760536
Reported geneMED13L
Mapped geneLOC105370003
Upstream gene id
Downstream gene id
SNP gene ids105370003
Upstream gene distance
Downstream gene distance
SNP risk allelers11067763-A
SNPsrs11067763
Merged0
SNP id current11067763
Contextintron_variant
Intergenic0
Allele frequency0.62
P value0.000000000000000002
Pvalue mlog17.698970004336
P value text
Or beta0.51
%95 Ci[0.39-0.63] unit increase
PlatformAffymetrix, Illumina [2485448] (imputed)
CNVN
Mapped traitdiastolic blood pressure
Mapped trait URIhttp://www.ebi.ac.uk/efo/EFO_0006336
Study accessionGCST002631
PubMed ID25249183
JournalHum Mol Genet
Linkwww.ncbi.nlm.nih.gov/pubmed/25249183
StudyGenome-wide association study in Chinese identifies novel loci for blood pressure and hypertension.
Disease/TraitHypertension
Initial sample5,065 Han Chinese ancestry cases, 4,404 Han Chinese ancestry controls
Replication sample29,799 Han Chinese ancestry cases, 39,347 Han Chinese ancestry controls
Region12q24.21
Chromosome idchr12
Chromosome position115760536
Reported geneMED13L
Mapped geneLOC105370003
Upstream gene id
Downstream gene id
SNP gene ids105370003
Upstream gene distance
Downstream gene distance
SNP risk allelers11067763-A
SNPsrs11067763
Merged0
SNP id current11067763
Contextintron_variant
Intergenic0
Allele frequency0.62
P value0.0000001
Pvalue mlog7
P value text
Or beta
%95 Ci
PlatformAffymetrix, Illumina [2485448] (imputed)
CNVN
Mapped traithypertension
Mapped trait URIhttp://www.ebi.ac.uk/efo/EFO_0000537
Study accessionGCST002627