Human SNP ID | rs2393895 |
---|---|
Human chromosome | chr10 |
Human SNP position | 62579087 |
Pig chromosome | chr14 |
Pig SNP position | 71311912 |
PubMed ID | 25534755 |
---|---|
Journal | Biol Psychiatry |
Link | www.ncbi.nlm.nih.gov/pubmed/25534755 |
Study | A Genome-wide Association Study of Autism Using the Simons Simplex Collection: Does Reducing Phenotypic Heterogeneity in Autism Increase Genetic Homogeneity? |
Disease/Trait | Autism spectrum disorder-related traits |
Initial sample | 1633 European ancestry trios, 942 trios |
Replication sample | NA |
Region | 10q21.2 |
Chromosome id | chr10 |
Chromosome position | 62579087 |
Reported gene | ZNF365 |
Mapped gene | ZNF365 |
Upstream gene id | |
Downstream gene id | |
SNP gene ids | 22891 |
Upstream gene distance | |
Downstream gene distance | |
SNP risk allele | rs2393895-? |
SNPs | rs2393895 |
Merged | 0 |
SNP id current | 2393895 |
Context | intron_variant |
Intergenic | 0 |
Allele frequency | NR |
P value | 0.0000002 |
Pvalue mlog | 6.69897000433601 |
P value text | (Higher ADOS social affect impairment) |
Or beta | 1.91 |
%95 Ci | [1.48-2.47] |
Platform | Illumina [up to 2017939] |
CNV | N |
Mapped trait | autism spectrum disorder symptom |
Mapped trait URI | http://www.ebi.ac.uk/efo/EFO_0005426 |
Study accession | GCST002639 |