Human SNP ID | rs10510837 |
---|---|
Human chromosome | chr3 |
Human SNP position | 60304113 |
Pig chromosome | chr13 |
Pig SNP position | 46054608 |
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 | 3p14.2 |
Chromosome id | chr3 |
Chromosome position | 60304113 |
Reported gene | FHIT |
Mapped gene | FHIT |
Upstream gene id | |
Downstream gene id | |
SNP gene ids | 2272 |
Upstream gene distance | |
Downstream gene distance | |
SNP risk allele | rs10510837-? |
SNPs | rs10510837 |
Merged | 0 |
SNP id current | 10510837 |
Context | intron_variant |
Intergenic | 0 |
Allele frequency | 0.12 |
P value | 0.000004 |
Pvalue mlog | 5.39794000867203 |
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 |