Human SNP ID | rs11099864 |
---|---|
Human chromosome | chr4 |
Human SNP position | 152972202 |
Pig chromosome | chr8 |
Pig SNP position | 80680473 |
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 | 4q31.3 |
Chromosome id | chr4 |
Chromosome position | 152972202 |
Reported gene | KIAA1727 |
Mapped gene | FHDC1 |
Upstream gene id | |
Downstream gene id | |
SNP gene ids | 85462 |
Upstream gene distance | |
Downstream gene distance | |
SNP risk allele | rs11099864-? |
SNPs | rs11099864 |
Merged | 0 |
SNP id current | 11099864 |
Context | intron_variant |
Intergenic | 0 |
Allele frequency | NR |
P value | 0.000009 |
Pvalue mlog | 5.04575749056067 |
P value text | |
Or beta | 1 |
%95 Ci | [0.80-1.40] |
Platform | Illumina [549062] |
CNV | N |
Mapped trait | amyotrophic lateral sclerosis |
Mapped trait URI | http://www.ebi.ac.uk/efo/EFO_0000253 |
Study accession | GCST000013 |