SNP Detail For rs2935776
1.Mapping Information
Human SNP ID rs2935776
Human chromosome chr8
Human SNP position 108617674
Pig chromosome chr4
Pig SNP position 31248094
2.Annotation Information
PubMed ID20932310
JournalBMC Neurol
Linkwww.ncbi.nlm.nih.gov/pubmed/20932310
StudyGenome-wide association reveals genetic effects on human Aβ42 and τ protein levels in cerebrospinal fluids: a case control study.
Disease/TraitCerebrospinal T-tau levels
Initial sample172 European ancestry Alzheimer__s disease cases, 109 European ancestry mild cognitive impairment cases, 109 European ancestry controls
Replication sampleNA
Region8q23.1
Chromosome idchr8
Chromosome position108617674
Reported geneintergenic
Mapped geneLOC101060000 - LOC101060002
Upstream gene id101060000
Downstream gene id101060002
SNP gene ids
Upstream gene distance217
Downstream gene distance27972
SNP risk allelers2935776-C
SNPsrs2935776
Merged0
SNP id current2935776
Contextintron_variant
Intergenic1
Allele frequencyNR
P value0.0000006
Pvalue mlog6.22184874961635
P value text(Controls)
Or beta
%95 Ci
PlatformIllumina [498205]
CNVN
Mapped traitt-tau measurement
Mapped trait URIhttp://www.ebi.ac.uk/efo/EFO_0004760
Study accessionGCST000826