SNP Detail For rs10492681
1.Mapping Information
Human SNP ID rs10492681
Human chromosome chr13
Human SNP position 40233346
Pig chromosome JH118429-1
Pig SNP position 10711
2.Annotation Information
PubMed ID17903293
JournalBMC Med Genet
Linkwww.ncbi.nlm.nih.gov/pubmed/17903293
StudyGenome-wide association with select biomarker traits in the Framingham Heart Study.
Disease/TraitSelect biomarker traits
Initial sample1,012 European ancestry individuals
Replication sampleNA
Region13q14.11
Chromosome idchr13
Chromosome position40233346
Reported geneintergenic
Mapped geneLOC105370172
Upstream gene id
Downstream gene id
SNP gene ids105370172
Upstream gene distance
Downstream gene distance
SNP risk allelers10492681-?
SNPsrs10492681
Merged0
SNP id current10492681
Contextintron_variant
Intergenic0
Allele frequencyNR
P value0.000002
Pvalue mlog5.69897000433601
P value text(ALT)
Or beta
%95 Ci
PlatformAffymetrix [70897]
CNVN
Mapped traitserum alanine aminotransferase measurement
Mapped trait URIhttp://www.ebi.ac.uk/efo/EFO_0004735
Study accessionGCST000083