SNP Detail For rs4460308
1.Mapping Information
Human SNP ID rs4460308
Human chromosome chr7
Human SNP position 104779613
Pig chromosome chr9
Pig SNP position 115283389
2.Annotation Information
PubMed ID24564958
JournalMol Autism
Linkwww.ncbi.nlm.nih.gov/pubmed/24564958
StudyVariability in the common genetic architecture of social-communication spectrum phenotypes during childhood and adolescence.
Disease/TraitSocial communication problems
Initial sampleUp to 5,628 European ancestry individuals
Replication sampleNA
Region7q22.2
Chromosome idchr7
Chromosome position104779613
Reported geneLHFPL3
Mapped geneLHFPL3
Upstream gene id
Downstream gene id
SNP gene ids375612
Upstream gene distance
Downstream gene distance
SNP risk allelers4460308-C
SNPsrs4460308
Merged0
SNP id current4460308
Contextintron_variant
Intergenic0
Allele frequency0.36
P value0.000006
Pvalue mlog5.22184874961635
P value text(Age 8)
Or beta0.11
%95 Ci[0.051-0.169] unit increase
PlatformIllumina [2293137] (imputed)
CNVN
Mapped traitsocial communication impairment
Mapped trait URIhttp://www.ebi.ac.uk/efo/EFO_0005427
Study accessionGCST002367