rs910049
From SNPedia
| Orientation | minus |
| Stabilized | minus |
| Make rs910049(A;A) |
| Make rs910049(A;G) |
| Make rs910049(G;G) |
| Reference | GRCh38 38.1/141 |
| Chromosome | 6 |
| Position | 32347950 |
| Gene | C6orf10, LOC101929163 |
| is a | snp |
| is | mentioned by |
| dbSNP | rs910049 |
| dbSNP (classic) | rs910049 |
| ClinGen | rs910049 |
| ebi | rs910049 |
| HLI | rs910049 |
| Exac | rs910049 |
| Gnomad | rs910049 |
| Varsome | rs910049 |
| LitVar | rs910049 |
| Map | rs910049 |
| PheGenI | rs910049 |
| Biobank | rs910049 |
| 1000 genomes | rs910049 |
| hgdp | rs910049 |
| ensembl | rs910049 |
| geneview | rs910049 |
| scholar | rs910049 |
| rs910049 | |
| pharmgkb | rs910049 |
| gwascentral | rs910049 |
| openSNP | rs910049 |
| 23andMe | rs910049 |
| SNPshot | rs910049 |
| SNPdbe | rs910049 |
| MSV3d | rs910049 |
| GWAS Ctlg | rs910049 |
| GMAF | 0.2163 |
| Max Magnitude | 0 |
| ? | (A;A) (A;G) (G;G) | 28 |
|---|---|---|
|
| ||
Repeatedly associated in genome association studies with type-2 diabetes, type-1 diabetes, multiple sclerosis, and coronary artery disease, according to [PMID 19161620
]
[PMID 17660530] Risk alleles for multiple sclerosis identified by a genomewide study.
[PMID 20546594] An application of Random Forests to a genome-wide association dataset: methodological considerations & new findings.
| GWAS snp | |
|---|---|
| PMID | [PMID 23321320] |
| Trait | Hepatitis C induced liver cirrhosis |
| Title | A genome-wide association study of HCV-induced liver cirrhosis in the Japanese population identifies novel susceptibility loci at the MHC region. |
| Risk Allele | A |
| P-val | 9E-11 |
| Odds Ratio | 1.46 [1.28-1.62] |
