Human SNP ID | rs13268726 |
---|---|
Human chromosome | chr8 |
Human SNP position | 125000892 |
Pig chromosome | chr4 |
Pig SNP position | 15275369 |
PubMed ID | 24931836 |
---|---|
Journal | Ann Neurol |
Link | www.ncbi.nlm.nih.gov/pubmed/24931836 |
Study | C9orf72 and UNC13A are shared risk loci for ALS and FTD: A genome-wide meta-analysis. |
Disease/Trait | Amyotrophic lateral sclerosis |
Initial sample | 4,377 European ancestry cases, 13,017 European ancestry controls |
Replication sample | NA |
Region | 8q24.13 |
Chromosome id | chr8 |
Chromosome position | 125000892 |
Reported gene | SQLE, KIAA0196, NSMCE2 |
Mapped gene | SQLE |
Upstream gene id | |
Downstream gene id | |
SNP gene ids | 6713 |
Upstream gene distance | |
Downstream gene distance | |
SNP risk allele | rs13268726-? |
SNPs | rs13268726 |
Merged | 0 |
SNP id current | 13268726 |
Context | intron_variant |
Intergenic | 0 |
Allele frequency | 0.1 |
P value | 0.000005 |
Pvalue mlog | 5.30102999566398 |
P value text | |
Or beta | 1.25 |
%95 Ci | [NR] |
Platform | Illumina [~ 1400000] (imputed) |
CNV | N |
Mapped trait | amyotrophic lateral sclerosis |
Mapped trait URI | http://www.ebi.ac.uk/efo/EFO_0000253 |
Study accession | GCST002509 |