SNP Detail For rs17750321
1.Mapping Information
Human SNP ID rs17750321
Human chromosome chr18
Human SNP position 37498719
Pig chromosome chr6
Pig SNP position 114126072
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
Region18q12.2
Chromosome idchr18
Chromosome position37498719
Reported geneBRUNOL4
Mapped geneCELF4
Upstream gene id
Downstream gene id
SNP gene ids56853
Upstream gene distance
Downstream gene distance
SNP risk allelers17750321-A
SNPsrs17750321
Merged0
SNP id current17750321
Contextintron_variant
Intergenic0
Allele frequency0.03
P value0.000005
Pvalue mlog5.30102999566398
P value text(Age 8)
Or beta0.3
%95 Ci[0.18-0.42] unit increase
PlatformIllumina [2293137] (imputed)
CNVN
Mapped traitsocial communication impairment
Mapped trait URIhttp://www.ebi.ac.uk/efo/EFO_0005427
Study accessionGCST002367