Human SNP ID | rs6013382 |
---|---|
Human chromosome | chr20 |
Human SNP position | 52086094 |
Pig chromosome | chr17 |
Pig SNP position | 59898835 |
PubMed ID | 17362836 |
---|---|
Journal | Lancet Neurol |
Link | www.ncbi.nlm.nih.gov/pubmed/17362836 |
Study | Genome-wide genotyping in amyotrophic lateral sclerosis and neurologically normal controls: first stage analysis and public release of data. |
Disease/Trait | Amyotrophic lateral sclerosis |
Initial sample | 276 European ancestry cases, 271 European ancestry controls |
Replication sample | NA |
Region | 20q13.2 |
Chromosome id | chr20 |
Chromosome position | 52086094 |
Reported gene | ZFP64 |
Mapped gene | ZFP64, LOC105372664 |
Upstream gene id | |
Downstream gene id | |
SNP gene ids | 55734, 105372664 |
Upstream gene distance | |
Downstream gene distance | |
SNP risk allele | rs6013382-? |
SNPs | rs6013382 |
Merged | 0 |
SNP id current | 6013382 |
Context | intron_variant |
Intergenic | 0 |
Allele frequency | NR |
P value | 0.000005 |
Pvalue mlog | 5.30102999566398 |
P value text | |
Or beta | 1.43 |
%95 Ci | [1.11-1.67] |
Platform | Illumina [549062] |
CNV | N |
Mapped trait | amyotrophic lateral sclerosis |
Mapped trait URI | http://www.ebi.ac.uk/efo/EFO_0000253 |
Study accession | GCST000013 |