Source: ALL
Variant Gene Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs3113494
rs3113494 		0.810 GeneticVariation BEFREE Although no SNPs reached genome-wide significance in the discovery phase for either phenotype, three SNPs were statistically significant in the replication analysis of ALS outcome: rs6080539 (177 kb from PCSK2), rs7000234 (4 kb from ZNF704), and rs3113494 (13 kb from LOC100506746). 22470424

2012
dbSNP: rs3113494
rs3113494 		0.810 GeneticVariation GWASCAT Although no SNPs reached genome-wide significance in the discovery phase for either phenotype, three SNPs were statistically significant in the replication analysis of ALS outcome: rs6080539 (177 kb from PCSK2), rs7000234 (4 kb from ZNF704), and rs3113494 (13 kb from LOC100506746). 22470424

2012
dbSNP: rs3113494
rs3113494 		0.810 GeneticVariation GWASDB Although no SNPs reached genome-wide significance in the discovery phase for either phenotype, three SNPs were statistically significant in the replication analysis of ALS outcome: rs6080539 (177 kb from PCSK2), rs7000234 (4 kb from ZNF704), and rs3113494 (13 kb from LOC100506746). 22470424

2012
dbSNP: rs4363506
rs4363506 		0.810 GeneticVariation BEFREE Our two-locus analysis showed that two two-locus combinations--rs4363506 (SNP1) and rs3733242 (SNP2), and rs4363506 and rs16984239 (SNP3) -- were significantly associated with sporadic ALS. 19740415

2009
dbSNP: rs4363506
rs4363506 		0.810 GeneticVariation GWASDB Genome-wide genotyping in amyotrophic lateral sclerosis and neurologically normal controls: first stage analysis and public release of data. 17362836

2007
dbSNP: rs4363506
rs4363506 		0.810 GeneticVariation GWASCAT Genome-wide genotyping in amyotrophic lateral sclerosis and neurologically normal controls: first stage analysis and public release of data. 17362836

2007
dbSNP: rs1971791
rs1971791 		G 0.800 GeneticVariation GWASCAT Age of onset of amyotrophic lateral sclerosis is modulated by a locus on 1p34.1. 22959728

2013
dbSNP: rs1971791
rs1971791 		G 0.800 GeneticVariation GWASDB Age of onset of amyotrophic lateral sclerosis is modulated by a locus on 1p34.1. 22959728

2013
dbSNP: rs5937496
rs5937496 		0.800 GeneticVariation GWASCAT Genome-wide association study identifies 19p13.3 (UNC13A) and 9p21.2 as susceptibility loci for sporadic amyotrophic lateral sclerosis. 19734901

2009
dbSNP: rs5937496
rs5937496 		0.800 GeneticVariation GWASDB Genome-wide association study identifies 19p13.3 (UNC13A) and 9p21.2 as susceptibility loci for sporadic amyotrophic lateral sclerosis. 19734901

2009
dbSNP: rs7577894
rs7577894 		T 0.800 GeneticVariation GWASCAT Reduced expression of the Kinesin-Associated Protein 3 (KIFAP3) gene increases survival in sporadic amyotrophic lateral sclerosis. 19451621

2009
dbSNP: rs7577894
rs7577894 		T 0.800 GeneticVariation GWASDB Reduced expression of the Kinesin-Associated Protein 3 (KIFAP3) gene increases survival in sporadic amyotrophic lateral sclerosis. 19451621

2009
dbSNP: rs855913
rs855913 		A 0.800 GeneticVariation GWASCAT Reduced expression of the Kinesin-Associated Protein 3 (KIFAP3) gene increases survival in sporadic amyotrophic lateral sclerosis. 19451621

2009
dbSNP: rs855913
rs855913 		A 0.800 GeneticVariation GWASDB Reduced expression of the Kinesin-Associated Protein 3 (KIFAP3) gene increases survival in sporadic amyotrophic lateral sclerosis. 19451621

2009
dbSNP: rs11224052
rs11224052 		T 0.700 GeneticVariation GWASCAT A genome-wide association study on amyotrophic lateral sclerosis in the Taiwanese Han population. 26580837

2016
dbSNP: rs1361121
rs1361121 		0.700 GeneticVariation GWASDB Residual association at C9orf72 suggests an alternative amyotrophic lateral sclerosis-causing hexanucleotide repeat. 23587638

2013
dbSNP: rs1517166
rs1517166 		0.700 GeneticVariation GWASDB Residual association at C9orf72 suggests an alternative amyotrophic lateral sclerosis-causing hexanucleotide repeat. 23587638

2013
dbSNP: rs1982915
rs1982915 		0.700 GeneticVariation GWASDB Residual association at C9orf72 suggests an alternative amyotrophic lateral sclerosis-causing hexanucleotide repeat. 23587638

2013
dbSNP: rs2453556
rs2453556 		0.700 GeneticVariation GWASDB Residual association at C9orf72 suggests an alternative amyotrophic lateral sclerosis-causing hexanucleotide repeat. 23587638

2013
dbSNP: rs2477518
rs2477518 		0.700 GeneticVariation GWASDB Residual association at C9orf72 suggests an alternative amyotrophic lateral sclerosis-causing hexanucleotide repeat. 23587638

2013
dbSNP: rs2785946
rs2785946 		A 0.700 GeneticVariation GWASCAT A genome-wide association study on amyotrophic lateral sclerosis in the Taiwanese Han population. 26580837

2016
dbSNP: rs2838568
rs2838568 		0.700 GeneticVariation GWASCAT Age of onset of amyotrophic lateral sclerosis is modulated by a locus on 1p34.1. 22959728

2013
dbSNP: rs284793
rs284793 		0.700 GeneticVariation GWASDB Genome-wide genotyping in amyotrophic lateral sclerosis and neurologically normal controls: first stage analysis and public release of data. 17362836

2007
dbSNP: rs7976059
rs7976059 		0.700 GeneticVariation GWASDB Genome-wide genotyping in amyotrophic lateral sclerosis and neurologically normal controls: first stage analysis and public release of data. 17362836

2007
dbSNP: rs945699
rs945699 		0.700 GeneticVariation GWASDB Whole-genome analysis of sporadic amyotrophic lateral sclerosis. 17671248

2007