SNP Detail For rs191241826
1.Mapping Information
Human SNP ID rs191241826
Human chromosome chr17
Human SNP position 40797075
Pig chromosome chr12
Pig SNP position 21825186
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/TraitCognitive decline rate in late mild cognitive impairment
Initial sample472 European ancestry cases, 47 cases
Replication sampleNA
Region17q21.2
Chromosome idchr17
Chromosome position40797075
Reported geneKRT28
Mapped geneKRT28
Upstream gene id
Downstream gene id
SNP gene ids162605
Upstream gene distance
Downstream gene distance
SNP risk allelers191241826-C
SNPsrs191241826
Merged
SNP id current191241826
Contextintron_variant
Intergenic0
Allele frequency0.01
P value0.000002
Pvalue mlog5.69897000433601
P value text(EA)
Or beta0.4843
%95 Ci[0.29-0.68] unit increase
PlatformIllumina [~ 9000000] (imputed)
CNVN
Mapped traitcognitive impairment, cognitive decline measurement
Mapped trait URIhttp://purl.obolibrary.org/obo/HP_0100543, http://www.ebi.ac.uk/efo/EFO_0007710
Study accessionGCST003075