Human SNP ID | rs892055 |
---|---|
Human chromosome | chr19 |
Human SNP position | 38422124 |
Pig chromosome | chr6 |
Pig SNP position | 42830803 |
PubMed ID | 21182207 |
---|---|
Journal | Autism Res |
Link | www.ncbi.nlm.nih.gov/pubmed/21182207 |
Study | Variants in several genomic regions associated with asperger disorder. |
Disease/Trait | Asperger disorder |
Initial sample | 848 individuals from 232 families |
Replication sample | NA |
Region | 19q13.2 |
Chromosome id | chr19 |
Chromosome position | 38422124 |
Reported gene | ODF3L2 |
Mapped gene | RASGRP4 |
Upstream gene id | |
Downstream gene id | |
SNP gene ids | 115727 |
Upstream gene distance | |
Downstream gene distance | |
SNP risk allele | rs892055-? |
SNPs | rs892055 |
Merged | 0 |
SNP id current | 892055 |
Context | missense_variant |
Intergenic | 0 |
Allele frequency | 0.33 |
P value | 0.000005 |
Pvalue mlog | 5.30102999566398 |
P value text | |
Or beta | |
%95 Ci | |
Platform | Illumina [439282] (imputed) |
CNV | N |
Mapped trait | Asperger syndrome |
Mapped trait URI | http://www.ebi.ac.uk/efo/EFO_0003757 |
Study accession | GCST000904 |