Human SNP ID | rs10850408 |
---|---|
Human chromosome | chr12 |
Human SNP position | 114942588 |
Pig chromosome | chr14 |
Pig SNP position | 39775846 |
PubMed ID | 22159054 |
---|---|
Journal | Arch Neurol |
Link | www.ncbi.nlm.nih.gov/pubmed/22159054 |
Study | A comprehensive genetic association study of Alzheimer disease in African Americans. |
Disease/Trait | Alzheimer__s disease |
Initial sample | 513 African American cases, 496 African American controls |
Replication sample | NA |
Region | 12q24.21 |
Chromosome id | chr12 |
Chromosome position | 114942588 |
Reported gene | intergenic |
Mapped gene | LOC105369999 - LOC102723639 |
Upstream gene id | 105369999 |
Downstream gene id | 102723639 |
SNP gene ids | |
Upstream gene distance | 206800 |
Downstream gene distance | 70599 |
SNP risk allele | rs10850408-? |
SNPs | rs10850408 |
Merged | 0 |
SNP id current | 10850408 |
Context | intergenic_variant |
Intergenic | 1 |
Allele frequency | NR |
P value | 0.0000009 |
Pvalue mlog | 6.04575749056067 |
P value text | |
Or beta | 1.59 |
%95 Ci | [1.32-1.92] |
Platform | Illumina [2505093] (imputed) |
CNV | N |
Mapped trait | Alzheimers disease |
Mapped trait URI | http://www.ebi.ac.uk/efo/EFO_0000249 |
Study accession | GCST001342 |