Human SNP ID | rs6683071 |
---|---|
Human chromosome | chr1 |
Human SNP position | 222750009 |
Pig chromosome | chr10 |
Pig SNP position | 13763888 |
PubMed ID | 19734545 |
---|---|
Journal | Hum Mol Genet |
Link | www.ncbi.nlm.nih.gov/pubmed/19734545 |
Study | A genome-wide study of common SNPs and CNVs in cognitive performance in the CANTAB. |
Disease/Trait | Cognitive performance |
Initial sample | Up to 1,295 individuals |
Replication sample | NA |
Region | 1q41 |
Chromosome id | chr1 |
Chromosome position | 222750009 |
Reported gene | FAM177B |
Mapped gene | FAM177B |
Upstream gene id | |
Downstream gene id | |
SNP gene ids | 400823 |
Upstream gene distance | |
Downstream gene distance | |
SNP risk allele | rs6683071-? |
SNPs | rs6683071 |
Merged | 0 |
SNP id current | 6683071 |
Context | missense_variant |
Intergenic | 0 |
Allele frequency | 0.2016 |
P value | 0.000004 |
Pvalue mlog | 5.39794000867203 |
P value text | (PC1) |
Or beta | |
%95 Ci | |
Platform | Illumina [475971] |
CNV | N |
Mapped trait | neuropsychological test |
Mapped trait URI | http://www.ebi.ac.uk/efo/EFO_0003926 |
Study accession | GCST000477 |