Human SNP ID | rs12044355 |
---|---|
Human chromosome | chr1 |
Human SNP position | 231708601 |
Pig chromosome | chr14 |
Pig SNP position | 63426247 |
PubMed ID | 19118814 |
---|---|
Journal | Am J Hum Genet |
Link | www.ncbi.nlm.nih.gov/pubmed/19118814 |
Study | Genome-wide association study implicates a chromosome 12 risk locus for late-onset Alzheimer disease. |
Disease/Trait | Alzheimer__s disease |
Initial sample | 492 European ancestry cases, 496 European ancestry controls |
Replication sample | 238 European ancestry cases, 220 European ancestry controls |
Region | 1q42.2 |
Chromosome id | chr1 |
Chromosome position | 231708601 |
Reported gene | DISC1 |
Mapped gene | DISC1, TSNAX-DISC1 |
Upstream gene id | |
Downstream gene id | |
SNP gene ids | 27185, 100303453 |
Upstream gene distance | |
Downstream gene distance | |
SNP risk allele | rs12044355-? |
SNPs | rs12044355 |
Merged | 0 |
SNP id current | 12044355 |
Context | intron_variant |
Intergenic | 0 |
Allele frequency | NR |
P value | 0.000009 |
Pvalue mlog | 5.04575749056067 |
P value text | |
Or beta | |
%95 Ci | |
Platform | Illumina [~ 2500000] (imputed) |
CNV | N |
Mapped trait | Alzheimers disease |
Mapped trait URI | http://www.ebi.ac.uk/efo/EFO_0000249 |
Study accession | GCST000310 |