Human SNP ID | rs4818184 |
---|---|
Human chromosome | chr21 |
Human SNP position | 40830505 |
Pig chromosome | chr13 |
Pig SNP position | 214454573 |
PubMed ID | 25226531 |
---|---|
Journal | Nat Commun |
Link | www.ncbi.nlm.nih.gov/pubmed/25226531 |
Study | Common variation near ROBO2 is associated with expressive vocabulary in infancy. |
Disease/Trait | Expressive vocabulary in infants |
Initial sample | 6,851 European ancestry 15-18-month-old children, 6,299 European ancestry 24-30-month-old children |
Replication sample | 2,038 European ancestry 15-18-month-old children, 4,520 European ancestry 24-30-month-old children |
Region | 21q22.2 |
Chromosome id | chr21 |
Chromosome position | 40830505 |
Reported gene | NR |
Mapped gene | DSCAM |
Upstream gene id | |
Downstream gene id | |
SNP gene ids | 1826 |
Upstream gene distance | |
Downstream gene distance | |
SNP risk allele | rs4818184-A |
SNPs | rs4818184 |
Merged | 0 |
SNP id current | 4818184 |
Context | intron_variant |
Intergenic | 0 |
Allele frequency | 0.13 |
P value | 0.000007 |
Pvalue mlog | 5.15490195998574 |
P value text | (15-18 months) |
Or beta | 0.1 |
%95 Ci | [0.057-0.143] unit decrease |
Platform | Illumina [2449665] (imputed) |
CNV | N |
Mapped trait | infant expressive language ability |
Mapped trait URI | http://www.ebi.ac.uk/efo/EFO_0006316 |
Study accession | GCST002611 |