rs4799088
From SNPedia
| Orientation | plus |
| Stabilized | plus |
| Make rs4799088(A;A) |
| Make rs4799088(A;G) |
| Make rs4799088(G;G) |
| Reference | GRCh38 38.1/141 |
| Chromosome | 18 |
| Position | 79813548 |
| Gene | KCNG2 |
| is a | snp |
| is | mentioned by |
| dbSNP | rs4799088 |
| dbSNP (classic) | rs4799088 |
| ClinGen | rs4799088 |
| ebi | rs4799088 |
| HLI | rs4799088 |
| Exac | rs4799088 |
| Gnomad | rs4799088 |
| Varsome | rs4799088 |
| LitVar | rs4799088 |
| Map | rs4799088 |
| PheGenI | rs4799088 |
| Biobank | rs4799088 |
| 1000 genomes | rs4799088 |
| hgdp | rs4799088 |
| ensembl | rs4799088 |
| geneview | rs4799088 |
| scholar | rs4799088 |
| rs4799088 | |
| pharmgkb | rs4799088 |
| gwascentral | rs4799088 |
| openSNP | rs4799088 |
| 23andMe | rs4799088 |
| SNPshot | rs4799088 |
| SNPdbe | rs4799088 |
| MSV3d | rs4799088 |
| GWAS Ctlg | rs4799088 |
| GMAF | 0.376 |
| Max Magnitude | 0 |
| ? | (A;A) (A;G) (G;G) | 28 |
|---|---|---|
|
| ||
| GWAS snp | |
|---|---|
| PMID | [PMID 20801717 ]
|
| Trait | |
| Title | Chromosome 9p21 in sporadic amyotrophic lateral sclerosis in the UK and seven other countries: a genome-wide association study |
| Risk Allele | |
| P-val | 0.000009 |
| Odds Ratio | 1.1500 [NR] |
