SNP Detail For rs3766680
1.Mapping Information
Human SNP ID rs3766680
Human chromosome chr1
Human SNP position 175327312
Pig chromosome chr9
Pig SNP position 129119485
2.Annotation Information
PubMed ID17903302
JournalBMC Med Genet
Linkwww.ncbi.nlm.nih.gov/pubmed/17903302
StudyFramingham Heart Study 100K Project: genome-wide associations for blood pressure and arterial stiffness.
Disease/TraitTonometry
Initial sample644 individuals
Replication sampleNA
Region1q25.1
Chromosome idchr1
Chromosome position175327312
Reported geneTNR
Mapped geneTNR
Upstream gene id
Downstream gene id
SNP gene ids7143
Upstream gene distance
Downstream gene distance
SNP risk allelers3766680-?
SNPsrs3766680
Merged0
SNP id current3766680
Contextintron_variant
Intergenic0
Allele frequencyNR
P value0.000004
Pvalue mlog5.39794000867203
P value text(FWLTA)
Or beta
%95 Ci
PlatformAffymetrix [70897]
CNVN
Mapped traitblood pressure
Mapped trait URIhttp://www.ebi.ac.uk/efo/EFO_0004325
Study accessionGCST000107