Human SNP ID | rs11921451 |
---|---|
Human chromosome | chr3 |
Human SNP position | 127068316 |
Pig chromosome | chr13 |
Pig SNP position | 80444449 |
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 | 3q21.3 |
Chromosome id | chr3 |
Chromosome position | 127068316 |
Reported gene | C3orf56 |
Mapped gene | LOC105374092 - C3orf56 |
Upstream gene id | 105374092 |
Downstream gene id | 285311 |
SNP gene ids | |
Upstream gene distance | 24880 |
Downstream gene distance | 124815 |
SNP risk allele | rs11921451-? |
SNPs | rs11921451 |
Merged | 0 |
SNP id current | 11921451 |
Context | intergenic_variant |
Intergenic | 1 |
Allele frequency | |
P value | 0.000005 |
Pvalue mlog | 5.30102999566398 |
P value text | |
Or beta | |
%95 Ci | |
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 |