SNP Detail For rs113027826
1.Mapping Information
Human SNP ID rs113027826
Human chromosome chr2
Human SNP position 206684788
Pig chromosome chr13
Pig SNP position 210991525
2.Annotation Information
PubMed ID26252872
JournalPLoS One
Linkwww.ncbi.nlm.nih.gov/pubmed/26252872
StudyVariations in the FRA10AC1 Fragile Site and 15q21 Are Associated with Cerebrospinal Fluid Aå°¾1-42 Level.
Disease/TraitCerebrospinal fluid t-tau:AB1-42 ratio
Initial sampleup to 189 European and other ancestry early mild cognitive impairment cases, up to 251 European and other ancestry late mild cognitive impairment cases, up to 121 European and other ancestry Alzheimer__s disease cases, up to 215 European and other ance
Replication sampleup to 3 European and other ancestry significant memory concern cases, up to 57 European and other ancestry early mild cognitive impairment cases, up to 61 European and other ancestry late mild cognitive impairment cases, up to 62 European and other an
Region2q33.3
Chromosome idchr2
Chromosome position206684788
Reported geneDYTN
Mapped geneDYTN
Upstream gene id
Downstream gene id
SNP gene ids391475
Upstream gene distance
Downstream gene distance
SNP risk allelers113027826-T
SNPsrs113027826
Merged
SNP id current113027826
Contextintron_variant
Intergenic0
Allele frequency0.14
P value0.0000004
Pvalue mlog6.39794000867203
P value text
Or beta0.4164
%95 Ci[NR] unit decrease
PlatformIllumina [~ 9000000] (imputed)
CNVN
Mapped traitt-tau:beta-amyloid 1-42 ratio measurement
Mapped trait URIhttp://www.ebi.ac.uk/efo/EFO_0007708
Study accessionGCST003079