SNP Detail For rs114685215
1.Mapping Information
Human SNP ID rs114685215
Human chromosome chr1
Human SNP position 112526100
Pig chromosome chr4
Pig SNP position 117971226
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/TraitCerebral amyloid deposition in APOEe4 non-carriers (PET imaging)
Initial sample370 European and other ancestry APOEe4 non-carriers
Replication sampleNA
Region1p13.2
Chromosome idchr1
Chromosome position112526100
Reported geneST7L
Mapped geneST7L
Upstream gene id
Downstream gene id
SNP gene ids54879
Upstream gene distance
Downstream gene distance
SNP risk allelers114685215-G
SNPsrs114685215
Merged
SNP id current114685215
Contextsynonymous_variant
Intergenic0
Allele frequency0.01
P value0.0000002
Pvalue mlog6.69897000433601
P value text
Or beta0.3389
%95 Ci[NR] unit decrease
PlatformIllumina [~ 9000000] (imputed)
CNVN
Mapped traitcerebral amyloid deposition measurement
Mapped trait URIhttp://www.ebi.ac.uk/efo/EFO_0007707
Study accessionGCST003074