Human SNP ID | rs4218 |
---|---|
Human chromosome | chr15 |
Human SNP position | 59136459 |
Pig chromosome | chr1 |
Pig SNP position | 124901403 |
PubMed ID | 24047820 |
---|---|
Journal | Mol Autism |
Link | www.ncbi.nlm.nih.gov/pubmed/24047820 |
Study | Common variation contributes to the genetic architecture of social communication traits. |
Disease/Trait | Social communication problems |
Initial sample | 5,584 European ancestry children |
Replication sample | 1,364 European ancestry children |
Region | 15q22.2 |
Chromosome id | chr15 |
Chromosome position | 59136459 |
Reported gene | RNF111, MYO1E |
Mapped gene | MYO1E |
Upstream gene id | |
Downstream gene id | |
SNP gene ids | 4643 |
Upstream gene distance | |
Downstream gene distance | |
SNP risk allele | rs4218-G |
SNPs | rs4218 |
Merged | 0 |
SNP id current | 4218 |
Context | 3_prime_UTR_variant |
Intergenic | 0 |
Allele frequency | 0.29 |
P value | 0.0000001 |
Pvalue mlog | 7 |
P value text | |
Or beta | 0.1 |
%95 Ci | [0.063-0.137] unit increase |
Platform | Illumina [~ 2500000] (imputed) |
CNV | N |
Mapped trait | social communication impairment |
Mapped trait URI | http://www.ebi.ac.uk/efo/EFO_0005427 |
Study accession | GCST002194 |