SNP Detail For rs895767
1.Mapping Information
Human SNP ID rs895767
Human chromosome chr2
Human SNP position 223158578
Pig chromosome chr15
Pig SNP position 138935294
2.Annotation Information
PubMed ID24468470
JournalNeurobiol Aging
Linkwww.ncbi.nlm.nih.gov/pubmed/24468470
StudyGenetic susceptibility to accelerated cognitive decline in the US Health and Retirement Study.
Disease/TraitCognitive decline (age-related)
Initial sample5,765 European ancestry individuals, 890 African American individuals
Replication sampleNA
Region2q36.1
Chromosome idchr2
Chromosome position223158578
Reported geneintergenic
Mapped geneLOC105373905 - LOC105373906
Upstream gene id105373905
Downstream gene id105373906
SNP gene ids
Upstream gene distance46189
Downstream gene distance44478
SNP risk allelers895767-?
SNPsrs895767
Merged0
SNP id current895767
Contextintron_variant
Intergenic1
Allele frequencyNR
P value0.000007
Pvalue mlog5.15490195998574
P value text(EA)
Or beta0.0102
%95 Ci[0.00572-0.01457] unit decrease
PlatformIllumina [1530316]
CNVN
Mapped traitcognitive decline
Mapped trait URIhttp://purl.obolibrary.org/obo/HP_0001268
Study accessionGCST002320