SNP Detail For rs770189
1.Mapping Information
Human SNP ID rs770189
Human chromosome chr5
Human SNP position 88792622
Pig chromosome chr2
Pig SNP position 98861348
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
Region5q14.3
Chromosome idchr5
Chromosome position88792622
Reported geneMEF2C
Mapped geneMEF2C
Upstream gene id
Downstream gene id
SNP gene ids4208
Upstream gene distance
Downstream gene distance
SNP risk allelers770189-?
SNPsrs770189
Merged0
SNP id current770189
Contextintron_variant
Intergenic0
Allele frequencyNR
P value0.000003
Pvalue mlog5.52287874528033
P value text(CB-PWV)
Or beta
%95 Ci
PlatformAffymetrix [70897]
CNVN
Mapped traitblood pressure
Mapped trait URIhttp://www.ebi.ac.uk/efo/EFO_0004325
Study accessionGCST000107