SNP Detail For rs932764
1.Mapping Information
Human SNP ID rs932764
Human chromosome chr10
Human SNP position 94136183
Pig chromosome chr14
Pig SNP position 115428971
2.Annotation Information
PubMed ID21909115
JournalNature
Linkwww.ncbi.nlm.nih.gov/pubmed/21909115
StudyGenetic variants in novel pathways influence blood pressure and cardiovascular disease risk.
Disease/TraitSystolic blood pressure
Initial sample69,395 European ancestry individuals
Replication sampleUp to 133,361 European ancestry individuals
Region10q23.33
Chromosome idchr10
Chromosome position94136183
Reported genePLCE1
Mapped genePLCE1
Upstream gene id
Downstream gene id
SNP gene ids51196
Upstream gene distance
Downstream gene distance
SNP risk allelers932764-G
SNPsrs932764
Merged0
SNP id current932764
Contextintron_variant
Intergenic0
Allele frequency0.44
P value0.0000000000000007
Pvalue mlog15.1549019599857
P value text
Or beta0.484
%95 Ci[NR] mmHg increase
PlatformAffymetrix, Illumina [~ 2500000] (imputed)
CNVN
Mapped traitsystolic blood pressure
Mapped trait URIhttp://www.ebi.ac.uk/efo/EFO_0006335
Study accessionGCST001227
PubMed ID21909115
JournalNature
Linkwww.ncbi.nlm.nih.gov/pubmed/21909115
StudyGenetic variants in novel pathways influence blood pressure and cardiovascular disease risk.
Disease/TraitDiastolic blood pressure
Initial sample69,395 European ancestry individuals
Replication sampleUp to 133,361 European ancestry individuals
Region10q23.33
Chromosome idchr10
Chromosome position94136183
Reported genePLCE1
Mapped genePLCE1
Upstream gene id
Downstream gene id
SNP gene ids51196
Upstream gene distance
Downstream gene distance
SNP risk allelers932764-G
SNPsrs932764
Merged0
SNP id current932764
Contextintron_variant
Intergenic0
Allele frequency0.44
P value0.0000008
Pvalue mlog6.09691001300805
P value text
Or beta0.185
%95 Ci[NR] mmHg increase
PlatformAffymetrix, Illumina [~ 2500000] (imputed)
CNVN
Mapped traitdiastolic blood pressure
Mapped trait URIhttp://www.ebi.ac.uk/efo/EFO_0006336
Study accessionGCST001228
PubMed ID21909115
JournalNature
Linkwww.ncbi.nlm.nih.gov/pubmed/21909115
StudyGenetic variants in novel pathways influence blood pressure and cardiovascular disease risk.
Disease/TraitHypertension
Initial sample69,395 European ancestry individuals
Replication sampleUp to 133,361 European ancestry individuals
Region10q23.33
Chromosome idchr10
Chromosome position94136183
Reported genePLCE1
Mapped genePLCE1
Upstream gene id
Downstream gene id
SNP gene ids51196
Upstream gene distance
Downstream gene distance
SNP risk allelers932764-G
SNPsrs932764
Merged0
SNP id current932764
Contextintron_variant
Intergenic0
Allele frequency0.44
P value0.000000009
Pvalue mlog8.04575749056067
P value text
Or beta0.055
%95 Ci[NR] unit increase
PlatformAffymetrix, Illumina [~ 2500000] (imputed)
CNVN
Mapped traithypertension
Mapped trait URIhttp://www.ebi.ac.uk/efo/EFO_0000537
Study accessionGCST001238