SNP Detail For rs892055
1.Mapping Information
Human SNP ID rs892055
Human chromosome chr19
Human SNP position 38422124
Pig chromosome chr6
Pig SNP position 42830803
2.Annotation Information
PubMed ID21182207
JournalAutism Res
Linkwww.ncbi.nlm.nih.gov/pubmed/21182207
StudyVariants in several genomic regions associated with asperger disorder.
Disease/TraitAsperger disorder
Initial sample848 individuals from 232 families
Replication sampleNA
Region19q13.2
Chromosome idchr19
Chromosome position38422124
Reported geneODF3L2
Mapped geneRASGRP4
Upstream gene id
Downstream gene id
SNP gene ids115727
Upstream gene distance
Downstream gene distance
SNP risk allelers892055-?
SNPsrs892055
Merged0
SNP id current892055
Contextmissense_variant
Intergenic0
Allele frequency0.33
P value0.000005
Pvalue mlog5.30102999566398
P value text
Or beta
%95 Ci
PlatformIllumina [439282] (imputed)
CNVN
Mapped traitAsperger syndrome
Mapped trait URIhttp://www.ebi.ac.uk/efo/EFO_0003757
Study accessionGCST000904