rs2814707
|
|
|
0.830 |
GeneticVariation |
BEFREE |
Recently, four single nucleotide polymorphisms (SNPs), including rs2814707 in the 9p21, rs12608932 in the UNC13A gene, rs13048019 in the TIMA1 gene, and rs2228576 in the SCNN1A gene have been reported to be associated with the risk for developing amyotrophic lateral sclerosis (ALS) in Caucasian population.
|
24493373 |
2014 |
rs2814707
|
|
|
0.830 |
GeneticVariation |
GWASDB |
Residual association at C9orf72 suggests an alternative amyotrophic lateral sclerosis-causing hexanucleotide repeat.
|
23587638 |
2013 |
rs2814707
|
|
|
0.830 |
GeneticVariation |
BEFREE |
We performed a replication study of the 2 genetic variants, rs2814707 on 9p21.2 and rs12608932 on 19p13.3 that are recently reported to be most significantly associated with sporadic amyotrophic lateral sclerosis (ALS) in Caucasians.
|
21295378 |
2011 |
rs2814707
|
|
|
0.830 |
GeneticVariation |
BEFREE |
In the joint analysis, which included samples from 4312 patients with ALS and 8425 control individuals, rs3849942 (p=4·64×10(-10); OR 1·22, 95% CI 1·15-1·30) and rs2814707 (p=4·72×10(-10); 1·22, 1·15-1·30) were associated with ALS.
|
20801717 |
2010 |
rs2814707
|
|
|
0.830 |
GeneticVariation |
GWASDB |
Chromosome 9p21 in amyotrophic lateral sclerosis in Finland: a genome-wide association study.
|
20801718 |
2010 |
rs2814707
|
|
|
0.830 |
GeneticVariation |
GWASDB |
Genome-wide association study identifies 19p13.3 (UNC13A) and 9p21.2 as susceptibility loci for sporadic amyotrophic lateral sclerosis.
|
19734901 |
2009 |
rs2814707
|
|
|
0.830 |
GeneticVariation |
GWASCAT |
Genome-wide association study identifies 19p13.3 (UNC13A) and 9p21.2 as susceptibility loci for sporadic amyotrophic lateral sclerosis.
|
19734901 |
2009 |