Human SNP ID | rs2352908 |
---|---|
Human chromosome | chr14 |
Human SNP position | 48968728 |
Pig chromosome | chr1 |
Pig SNP position | 199408301 |
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 | 14q21.3 |
Chromosome id | chr14 |
Chromosome position | 48968728 |
Reported gene | intergenic |
Mapped gene | LOC105370483 - LOC105378178 |
Upstream gene id | 105370483 |
Downstream gene id | 105378178 |
SNP gene ids | |
Upstream gene distance | 539480 |
Downstream gene distance | 86915 |
SNP risk allele | rs2352908-G |
SNPs | rs2352908 |
Merged | 0 |
SNP id current | 2352908 |
Context | intergenic_variant |
Intergenic | 1 |
Allele frequency | 0.84 |
P value | 0.000001 |
Pvalue mlog | 6 |
P value text | |
Or beta | 0.12 |
%95 Ci | [0.071-0.169] 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 |