SNP Detail For rs133885
1.Mapping Information
Human SNP ID rs133885
Human chromosome chr22
Human SNP position 25763322
Pig chromosome chr14
Pig SNP position 46293628
2.Annotation Information
PubMed ID23423138
JournalTransl Psychiatry
Linkwww.ncbi.nlm.nih.gov/pubmed/23423138
StudyA common variant in myosin-18B contributes to mathematical abilities in children with dyslexia and intraparietal sulcus variability in adults.
Disease/TraitMathematical ability in children with dyslexia
Initial sample200 European ancestry cases
Replication sample510 European ancestry cases
Region22q12.1
Chromosome idchr22
Chromosome position25763322
Reported geneMYO18B
Mapped geneMYO18B
Upstream gene id
Downstream gene id
SNP gene ids84700
Upstream gene distance
Downstream gene distance
SNP risk allelers133885-?
SNPsrs133885
Merged0
SNP id current133885
Contextmissense_variant
Intergenic0
Allele frequencyNR
P value0.0000000008
Pvalue mlog9.09691001300805
P value text
Or beta4.87
%95 Ci% increase
PlatformIllumina [NR]
CNVN
Mapped traitmathematical ability
Mapped trait URIhttp://www.ebi.ac.uk/efo/EFO_0004875
Study accessionGCST001866