Human SNP ID | rs895767 |
---|---|
Human chromosome | chr2 |
Human SNP position | 223158578 |
Pig chromosome | chr15 |
Pig SNP position | 138935294 |
PubMed ID | 24468470 |
---|---|
Journal | Neurobiol Aging |
Link | www.ncbi.nlm.nih.gov/pubmed/24468470 |
Study | Genetic susceptibility to accelerated cognitive decline in the US Health and Retirement Study. |
Disease/Trait | Cognitive decline (age-related) |
Initial sample | 5,765 European ancestry individuals, 890 African American individuals |
Replication sample | NA |
Region | 2q36.1 |
Chromosome id | chr2 |
Chromosome position | 223158578 |
Reported gene | intergenic |
Mapped gene | LOC105373905 - LOC105373906 |
Upstream gene id | 105373905 |
Downstream gene id | 105373906 |
SNP gene ids | |
Upstream gene distance | 46189 |
Downstream gene distance | 44478 |
SNP risk allele | rs895767-? |
SNPs | rs895767 |
Merged | 0 |
SNP id current | 895767 |
Context | intron_variant |
Intergenic | 1 |
Allele frequency | NR |
P value | 0.000007 |
Pvalue mlog | 5.15490195998574 |
P value text | (EA) |
Or beta | 0.0102 |
%95 Ci | [0.00572-0.01457] unit decrease |
Platform | Illumina [1530316] |
CNV | N |
Mapped trait | cognitive decline |
Mapped trait URI | http://purl.obolibrary.org/obo/HP_0001268 |
Study accession | GCST002320 |