Rs16984239
From SNPedia
| Orientation | plus |
| is a | snp |
| is | mentioned by |
| dbSNP | rs16984239 |
| PheGenI | rs16984239 |
| nextbio | rs16984239 |
| hapmap | rs16984239 |
| 1000 genomes | rs16984239 |
| hgdp | rs16984239 |
| ensembl | rs16984239 |
| gopubmed | rs16984239 |
| geneview | rs16984239 |
| scholar | rs16984239 |
| rs16984239 | |
| pharmgkb | rs16984239 |
| gwascentral | rs16984239 |
| openSNP | rs16984239 |
| 23andMe | rs16984239 |
| 23andMe all | rs16984239 |
| SNP Nexus | |
| SNPshot | rs16984239 |
| SNPdbe | rs16984239 |
| MSV3d | rs16984239 |
| Chromosome | 2 |
| Orientation | plus |
| GMAF | 0.1699 |
| Position | 18234446 |
| Reference | GRCh37 37.1/131 |
| Max Magnitude |
| Make rs16984239(A;A) |
| Make rs16984239(A;C) |
| Make rs16984239(C;C) |
| ? | (A;A) (A;C) (C;C) | 28 |
|---|---|---|
| GWAS | |
|---|---|
| SNP | rs16984239 |
| PubMedID | [PMID 17362836] |
| Condition | Amyotrophic lateral sclerosis |
| Gene | Intergenic |
| Risk Allele | |
| pValue | 2.00E-006 |
| OR | 2.1 |
| 95% CI | 1.50-3.00 |
[PMID 19740415] Genome-wide association reveals three SNPs associated with sporadic amyotrophic lateral sclerosis through a two-locus analysis
[PMID 20823317] is-rSNP: a novel technique for in silico regulatory SNP detection.
| GET Evidence | |
|---|---|
| rs16984239 | |
| aa_change | |
| aa_change_short | |
| impact | pathogenic |
| qualified_impact | Insufficiently evaluated pathogenic |
| overall_frequency | 0.179688 |
| summary | |
