Human SNP ID | rs9518810 |
---|---|
Human chromosome | chr13 |
Human SNP position | 102691078 |
Pig chromosome | chr11 |
Pig SNP position | 78329198 |
PubMed ID | 25387704 |
---|---|
Journal | Psychophysiology |
Link | www.ncbi.nlm.nih.gov/pubmed/25387704 |
Study | Heritability and molecular-genetic basis of resting EEG activity: A genome-wide association study. |
Disease/Trait | Electroencephalogram traits |
Initial sample | 2,383 European ancestry adolescents and 1,643 European ancestry adults from 1,613 families |
Replication sample | NA |
Region | 13q33.1 |
Chromosome id | chr13 |
Chromosome position | 102691078 |
Reported gene | METTL21C |
Mapped gene | METTL21C |
Upstream gene id | |
Downstream gene id | |
SNP gene ids | 196541 |
Upstream gene distance | |
Downstream gene distance | |
SNP risk allele | rs9518810-? |
SNPs | rs9518810 |
Merged | 0 |
SNP id current | 9518810 |
Context | intron_variant |
Intergenic | 0 |
Allele frequency | NR |
P value | 0.000002 |
Pvalue mlog | 5.69897000433601 |
P value text | (Alpha power, Cz) |
Or beta | 0.174 |
%95 Ci | [0.1-0.25] unit decrease |
Platform | Illumina [527829] |
CNV | N |
Mapped trait | alpha wave measurement, electroencephalogram measurement |
Mapped trait URI | http://www.ebi.ac.uk/efo/EFO_0006870, http://www.ebi.ac.uk/efo/EFO_0004357 |
Study accession | GCST002709 |