SNP Detail For rs2393895
1.Mapping Information
Human SNP ID rs2393895
Human chromosome chr10
Human SNP position 62579087
Pig chromosome chr14
Pig SNP position 71311912
2.Annotation Information
PubMed ID25534755
JournalBiol Psychiatry
Linkwww.ncbi.nlm.nih.gov/pubmed/25534755
StudyA Genome-wide Association Study of Autism Using the Simons Simplex Collection: Does Reducing Phenotypic Heterogeneity in Autism Increase Genetic Homogeneity?
Disease/TraitAutism spectrum disorder-related traits
Initial sample1633 European ancestry trios, 942 trios
Replication sampleNA
Region10q21.2
Chromosome idchr10
Chromosome position62579087
Reported geneZNF365
Mapped geneZNF365
Upstream gene id
Downstream gene id
SNP gene ids22891
Upstream gene distance
Downstream gene distance
SNP risk allelers2393895-?
SNPsrs2393895
Merged0
SNP id current2393895
Contextintron_variant
Intergenic0
Allele frequencyNR
P value0.0000002
Pvalue mlog6.69897000433601
P value text(Higher ADOS social affect impairment)
Or beta1.91
%95 Ci[1.48-2.47]
PlatformIllumina [up to 2017939]
CNVN
Mapped traitautism spectrum disorder symptom
Mapped trait URIhttp://www.ebi.ac.uk/efo/EFO_0005426
Study accessionGCST002639