SNP Detail For rs7584755
1.Mapping Information
Human SNP ID rs7584755
Human chromosome chr2
Human SNP position 1911740
Pig chromosome chr3
Pig SNP position 141629560
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
Region2p25.3
Chromosome idchr2
Chromosome position1911740
Reported geneMYT1L
Mapped geneMYT1L
Upstream gene id
Downstream gene id
SNP gene ids23040
Upstream gene distance
Downstream gene distance
SNP risk allelers7584755-C
SNPsrs7584755
Merged
SNP id current7584755
Contextintron_variant
Intergenic0
Allele frequency0.03
P value0.0000003
Pvalue mlog6.52287874528033
P value text
Or beta0.4674
%95 Ci[0.29-0.64] unit decrease
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