Rs12680546
From SNPedia
| Orientation | plus |
| is a | snp |
| is | mentioned by |
| dbSNP | rs12680546 |
| PheGenI | rs12680546 |
| nextbio | rs12680546 |
| hapmap | rs12680546 |
| 1000 genomes | rs12680546 |
| hgdp | rs12680546 |
| ensembl | rs12680546 |
| gopubmed | rs12680546 |
| geneview | rs12680546 |
| scholar | rs12680546 |
| rs12680546 | |
| pharmgkb | rs12680546 |
| gwascentral | rs12680546 |
| openSNP | rs12680546 |
| 23andMe | rs12680546 |
| 23andMe all | rs12680546 |
| SNP Nexus | |
| SNPshot | rs12680546 |
| SNPdbe | rs12680546 |
| MSV3d | rs12680546 |
| Chromosome | 8 |
| Orientation | plus |
| GMAF | 0.1671 |
| Position | 136871739 |
| Reference | GRCh37 37.1/131 |
| Max Magnitude |
| Make rs12680546(A;A) |
| Make rs12680546(A;G) |
| Make rs12680546(G;G) |
| ? | (A;A) (A;G) (G;G) | 28 |
|---|---|---|
| GWAS | |
|---|---|
| SNP | rs12680546 |
| PubMedID | [PMID 17362836] |
| Condition | Amyotrophic lateral sclerosis |
| Gene | Intergenic |
| Risk Allele | |
| pValue | 3.00E-006 |
| OR | 1.67 |
| 95% CI | 1.25-2.00 |
[PMID 17052657] Genome-wide genotyping in Parkinson's disease and neurologically normal controls: first stage analysis and public release of data.
[PMID 19740415] Genome-wide association reveals three SNPs associated with sporadic amyotrophic lateral sclerosis through a two-locus analysis.
| GET Evidence | |
|---|---|
| rs12680546 | |
| aa_change | |
| aa_change_short | |
| impact | pathogenic |
| qualified_impact | Insufficiently evaluated pathogenic |
| overall_frequency | 0.210938 |
| summary | |
