SNP Detail For rs10496289
1.Mapping Information
Human SNP ID rs10496289
Human chromosome chr2
Human SNP position 83066256
Pig chromosome chr3
Pig SNP position 64265830
2.Annotation Information
PubMed ID21626137
JournalHum Genet
Linkwww.ncbi.nlm.nih.gov/pubmed/21626137
StudyTwo-marker association tests yield new disease associations for coronary artery disease and hypertension.
Disease/TraitHypertension
Initial sample~2,000 European ancestry cases, ~3,000 European ancestry controls
Replication sampleNA
Region2p12
Chromosome idchr2;2
Chromosome position83065441;83066256
Reported geneintergenic
Mapped geneLOC105374832 - LOC105374833; LOC105374832 - LOC105374833
Upstream gene id
Downstream gene id
SNP gene ids
Upstream gene distance
Downstream gene distance
SNP risk allelers10496288-G; rs10496289-C
SNPsrs10496288; rs10496289
Merged0
SNP id current
Contextintergenic_variant; intergenic_variant
Intergenic
Allele frequencyNR
P value0.000000002
Pvalue mlog8.69897000433601
P value text
Or beta
%95 Ci
PlatformAffymetrix [405022]
CNVN
Mapped traithypertension
Mapped trait URIhttp://www.ebi.ac.uk/efo/EFO_0000537
Study accessionGCST001085