SNP Detail For rs3761168
1.Mapping Information
Human SNP ID rs3761168
Human chromosome chr20
Human SNP position 8885071
Pig chromosome chr17
Pig SNP position 19950213
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
Region20p12.3
Chromosome idchr20
Chromosome position8885071
Reported genePLCB1
Mapped genePLCB1 - LOC105372522
Upstream gene id23236
Downstream gene id105372522
SNP gene ids
Upstream gene distance171
Downstream gene distance77128
SNP risk allelers3761168-A
SNPsrs3761168
Merged0
SNP id current3761168
Contextintron_variant
Intergenic1
Allele frequency0.05
P value0.00000008
Pvalue mlog7.09691001300805
P value text(Age 17)
Or beta0.32
%95 Ci[0.2-0.44] unit increase
PlatformIllumina [2293137] (imputed)
CNVN
Mapped traitsocial communication impairment
Mapped trait URIhttp://www.ebi.ac.uk/efo/EFO_0005427
Study accessionGCST002367