Human SNP ID | rs17393344 |
---|---|
Human chromosome | chr13 |
Human SNP position | 108821598 |
Pig chromosome | chr11 |
Pig SNP position | 83453071 |
PubMed ID | 23535033 |
---|---|
Journal | Alzheimers Dement |
Link | www.ncbi.nlm.nih.gov/pubmed/23535033 |
Study | Genome-wide association study of the rate of cognitive decline in Alzheimer__s disease. |
Disease/Trait | Alzheimer__s disease (cognitive decline) |
Initial sample | 303 European ancestry cases |
Replication sample | |
Region | 13q33.3 |
Chromosome id | chr13 |
Chromosome position | 108821598 |
Reported gene | MYO16 |
Mapped gene | MYO16 |
Upstream gene id | |
Downstream gene id | |
SNP gene ids | 23026 |
Upstream gene distance | |
Downstream gene distance | |
SNP risk allele | rs17393344-? |
SNPs | rs17393344 |
Merged | 0 |
SNP id current | 17393344 |
Context | intron_variant |
Intergenic | 0 |
Allele frequency | 0.06 |
P value | 0.00000002 |
Pvalue mlog | 7.69897000433601 |
P value text | |
Or beta | 0.26 |
%95 Ci | unit decrease |
Platform | Illumina [NR] (imputed) |
CNV | N |
Mapped trait | Alzheimers disease |
Mapped trait URI | http://www.ebi.ac.uk/efo/EFO_0000249 |
Study accession | GCST001915 |