rs6116492
From SNPedia
| Orientation | plus |
| Stabilized | plus |
| Geno | Mag | Summary |
|---|---|---|
| (G;G) | 0 |
| Make rs6116492(G;T) |
| Make rs6116492(T;T) |
| Reference | GRCh38 38.1/141 |
| Chromosome | 20 |
| Position | 4717980 |
| is a | snp |
| is | mentioned by |
| dbSNP | rs6116492 |
| dbSNP (classic) | rs6116492 |
| ClinGen | rs6116492 |
| ebi | rs6116492 |
| HLI | rs6116492 |
| Exac | rs6116492 |
| Gnomad | rs6116492 |
| Varsome | rs6116492 |
| LitVar | rs6116492 |
| Map | rs6116492 |
| PheGenI | rs6116492 |
| Biobank | rs6116492 |
| 1000 genomes | rs6116492 |
| hgdp | rs6116492 |
| ensembl | rs6116492 |
| geneview | rs6116492 |
| scholar | rs6116492 |
| rs6116492 | |
| pharmgkb | rs6116492 |
| gwascentral | rs6116492 |
| openSNP | rs6116492 |
| 23andMe | rs6116492 |
| SNPshot | rs6116492 |
| SNPdbe | rs6116492 |
| MSV3d | rs6116492 |
| GWAS Ctlg | rs6116492 |
| GMAF | 0.06612 |
| Max Magnitude | 0 |
| ? | (G;G) (G;T) (T;T) | 28 |
|---|---|---|
|
| ||
| GWAS snp | |
|---|---|
| PMID | [PMID 22137330] |
| Trait | |
| Title | Genome-wide study links MTMR7 gene to variant Creutzfeldt-Jakob risk. |
| Risk Allele | |
| P-val | 5E-7 |
| Odds Ratio | None None |
[PMID 19081515
] Genetic risk factors for variant Creutzfeldt-Jakob disease: a genome-wide association study.
