Variant Gene Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs3849942
rs3849942
A 0.870 GeneticVariation GWASDB The other was detected in a 232 kb block of linkage disequilibrium (rs3849942, p=9·11×10(-11)) in a region of chromosome 9p that was previously identified in linkage studies of families with ALS. 20801718

2010

dbSNP: rs3849942
rs3849942
A 0.870 GeneticVariation GWASDB Eight genomic regions provided evidence of association with ALS, including 9p21.2 (rs3849942, odds ratio [OR] = 1.21; p = 4.41 × 10(-7)), 17p11.2 (rs7477, OR = 1.30; p = 2.89 × 10(-7)), and 19p13 (rs12608932, OR = 1.37, p = 1.29 × 10(-7)). 22959728

2013

dbSNP: rs3849942
rs3849942
0.870 GeneticVariation GWASDB Genome-wide association testing was performed first using all samples, and then restricting the analysis to samples not carrying the mutation. rs3849942 and rs903603 were strongly associated with ALS when all samples were included (rs3849942, p = [3 × 2] × 10(-6), rank 7/442,057; rs903603, p = [7 × 6] × 10(-8), rank 2/442,057). 23587638

2013

dbSNP: rs3849942
rs3849942
0.870 GeneticVariation GWASDB Genome-wide association study identifies 19p13.3 (UNC13A) and 9p21.2 as susceptibility loci for sporadic amyotrophic lateral sclerosis. 19734901

2009

dbSNP: rs3849942
rs3849942
0.870 GeneticVariation GWASDB In this analysis, two single nucleotide polymorphisms in a locus on chromosome 9p21.2 were associated with ALS: rs3849942 (p=2·22×10(-6); odds ratio [OR] 1·39, 95% CI 1·21-1·59) and rs2814707 (p=3·32×10(-6); 1·38, 1·20-1·58). 20801717

2010

dbSNP: rs2814707
rs2814707
0.830 GeneticVariation GWASDB Residual association at C9orf72 suggests an alternative amyotrophic lateral sclerosis-causing hexanucleotide repeat. 23587638

2013

dbSNP: rs2814707
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

dbSNP: rs2814707
rs2814707
0.830 GeneticVariation GWASDB Chromosome 9p21 in amyotrophic lateral sclerosis in Finland: a genome-wide association study. 20801718

2010

dbSNP: rs10122902
rs10122902
0.800 GeneticVariation GWASDB Chromosome 9p21 in sporadic amyotrophic lateral sclerosis in the UK and seven other countries: a genome-wide association study. 20801717

2010

dbSNP: rs10757665
rs10757665
0.700 GeneticVariation GWASDB Residual association at C9orf72 suggests an alternative amyotrophic lateral sclerosis-causing hexanucleotide repeat. 23587638

2013

dbSNP: rs10812611
rs10812611
0.700 GeneticVariation GWASDB Residual association at C9orf72 suggests an alternative amyotrophic lateral sclerosis-causing hexanucleotide repeat. 23587638

2013

dbSNP: rs10967976
rs10967976
0.700 GeneticVariation GWASDB Residual association at C9orf72 suggests an alternative amyotrophic lateral sclerosis-causing hexanucleotide repeat. 23587638

2013

dbSNP: rs12349820
rs12349820
0.700 GeneticVariation GWASDB Residual association at C9orf72 suggests an alternative amyotrophic lateral sclerosis-causing hexanucleotide repeat. 23587638

2013

dbSNP: rs1565948
rs1565948
0.700 GeneticVariation GWASDB Residual association at C9orf72 suggests an alternative amyotrophic lateral sclerosis-causing hexanucleotide repeat. 23587638

2013

dbSNP: rs2282240
rs2282240
0.700 GeneticVariation GWASDB Residual association at C9orf72 suggests an alternative amyotrophic lateral sclerosis-causing hexanucleotide repeat. 23587638

2013

dbSNP: rs2282241
rs2282241
0.700 GeneticVariation GWASDB Residual association at C9orf72 suggests an alternative amyotrophic lateral sclerosis-causing hexanucleotide repeat. 23587638

2013

dbSNP: rs60242496
rs60242496
0.700 GeneticVariation GWASDB Residual association at C9orf72 suggests an alternative amyotrophic lateral sclerosis-causing hexanucleotide repeat. 23587638

2013

dbSNP: rs774357
rs774357
0.700 GeneticVariation GWASDB Residual association at C9orf72 suggests an alternative amyotrophic lateral sclerosis-causing hexanucleotide repeat. 23587638

2013

dbSNP: rs774359
rs774359
0.700 GeneticVariation GWASDB Chromosome 9p21 in amyotrophic lateral sclerosis in Finland: a genome-wide association study. 20801718

2010

dbSNP: rs774359
rs774359
0.700 GeneticVariation GWASDB Residual association at C9orf72 suggests an alternative amyotrophic lateral sclerosis-causing hexanucleotide repeat. 23587638

2013