Human SNP ID | rs11061269 |
---|---|
Human chromosome | chr12 |
Human SNP position | 130971904 |
Pig chromosome | chr14 |
Pig SNP position | 25765826 |
PubMed ID | 24529757 |
---|---|
Journal | Neurobiol Aging |
Link | www.ncbi.nlm.nih.gov/pubmed/24529757 |
Study | Genome-wide association study combining pathway analysis for typical sporadic amyotrophic lateral sclerosis in Chinese Han populations. |
Disease/Trait | Amyotrophic lateral sclerosis (sporadic) |
Initial sample | 250 Han Chinese ancestry cases, 250 Han Chinese ancestry controls |
Replication sample | NA |
Region | 12q24.33 |
Chromosome id | chr12 |
Chromosome position | 130971904 |
Reported gene | GPR133 |
Mapped gene | ADGRD1 |
Upstream gene id | |
Downstream gene id | |
SNP gene ids | 283383 |
Upstream gene distance | |
Downstream gene distance | |
SNP risk allele | rs11061269-? |
SNPs | rs11061269 |
Merged | 0 |
SNP id current | 11061269 |
Context | intron_variant |
Intergenic | 0 |
Allele frequency | 0.08 |
P value | 0.0000000008 |
Pvalue mlog | 9.09691001300805 |
P value text | |
Or beta | 3.7761 |
%95 Ci | [2.49-5.74] |
Platform | Illumina [859311] |
CNV | N |
Mapped trait | sporadic amyotrophic lateral sclerosis |
Mapped trait URI | http://www.ebi.ac.uk/efo/EFO_0001357 |
Study accession | GCST002337 |