SNP Detail For rs10488172
1.Mapping Information
Human SNP ID rs10488172
Human chromosome chr7
Human SNP position 133650423
Pig chromosome chr18
Pig SNP position 16530702
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
Region7q33
Chromosome idchr7
Chromosome position133650423
Reported geneEXOC4
Mapped geneEXOC4
Upstream gene id
Downstream gene id
SNP gene ids60412
Upstream gene distance
Downstream gene distance
SNP risk allelers10488172-?
SNPsrs10488172
Merged0
SNP id current10488172
Contextintron_variant
Intergenic0
Allele frequencyNR
P value0.000008
Pvalue mlog5.09691001300805
P value text(RWLTA)
Or beta
%95 Ci
PlatformAffymetrix [70897]
CNVN
Mapped traitblood pressure
Mapped trait URIhttp://www.ebi.ac.uk/efo/EFO_0004325
Study accessionGCST000107