Human SNP ID | rs17140547 |
---|---|
Human chromosome | chr11 |
Human SNP position | 80666008 |
Pig chromosome | chr9 |
Pig SNP position | 16697790 |
PubMed ID | 22903471 |
---|---|
Journal | Brain Imaging Behav |
Link | www.ncbi.nlm.nih.gov/pubmed/22903471 |
Study | Genome-wide association identifies genetic variants associated with lentiform nucleus volume in N = 1345 young and elderly subjects. |
Disease/Trait | Lentiform nucleus volume |
Initial sample | 162 European ancestry Alzheimer__s disease cases, 346 European ancestry mild cognitive impairment cases, 198 European ancestry controls, 639 European ancestry individuals from 364 families |
Replication sample | NA |
Region | 11q14.1 |
Chromosome id | chr11 |
Chromosome position | 80666008 |
Reported gene | intergenic |
Mapped gene | LOC101928964 |
Upstream gene id | |
Downstream gene id | |
SNP gene ids | 101928964 |
Upstream gene distance | |
Downstream gene distance | |
SNP risk allele | rs17140547-T |
SNPs | rs17140547 |
Merged | 0 |
SNP id current | 17140547 |
Context | intergenic_variant |
Intergenic | 0 |
Allele frequency | 0.02 |
P value | 0.000008 |
Pvalue mlog | 5.09691001300805 |
P value text | |
Or beta | 532.56 |
%95 Ci | [NR] unit decrease |
Platform | Illumina [2380200] (imputed) |
CNV | N |
Mapped trait | lentiform nucleus measurement |
Mapped trait URI | http://www.ebi.ac.uk/efo/EFO_0004913 |
Study accession | GCST001640 |