Human SNP ID | rs4280164 |
---|---|
Human chromosome | chr14 |
Human SNP position | 24302079 |
Pig chromosome | chr7 |
Pig SNP position | 80260243 |
PubMed ID | 24571439 |
---|---|
Journal | Genes Brain Behav |
Link | www.ncbi.nlm.nih.gov/pubmed/24571439 |
Study | Genome-wide association analyses of child genotype effects and parent-of-origin effects in specific language impairment. |
Disease/Trait | Parent of origin effect on language impairment (paternal) |
Initial sample | 153 European ancestry case-parent trios, 54 European ancestry case-mother duos, 12 European ancestry case-father duos, 18 European ancestry cases |
Replication sample | NA |
Region | 14q12 |
Chromosome id | chr14 |
Chromosome position | 24302079 |
Reported gene | C14orf21, DHRS1, CIDEB, ADCY4, LTB4R |
Mapped gene | NOP9 |
Upstream gene id | |
Downstream gene id | |
SNP gene ids | 161424 |
Upstream gene distance | |
Downstream gene distance | |
SNP risk allele | rs4280164-G |
SNPs | rs4280164 |
Merged | 0 |
SNP id current | 4280164 |
Context | missense_variant |
Intergenic | 0 |
Allele frequency | 0.767 |
P value | 0.00000004 |
Pvalue mlog | 7.39794000867203 |
P value text | |
Or beta | 3.872 |
%95 Ci | [NR] unit increase |
Platform | Illumina [614937] |
CNV | N |
Mapped trait | language impairment |
Mapped trait URI | http://www.ebi.ac.uk/efo/EFO_0005425 |
Study accession | GCST002371 |