SNP Detail For rs10510837
1.Mapping Information
Human SNP ID rs10510837
Human chromosome chr3
Human SNP position 60304113
Pig chromosome chr13
Pig SNP position 46054608
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
Region3p14.2
Chromosome idchr3
Chromosome position60304113
Reported geneFHIT
Mapped geneFHIT
Upstream gene id
Downstream gene id
SNP gene ids2272
Upstream gene distance
Downstream gene distance
SNP risk allelers10510837-?
SNPsrs10510837
Merged0
SNP id current10510837
Contextintron_variant
Intergenic0
Allele frequency0.12
P value0.000004
Pvalue mlog5.39794000867203
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