rs6904029
From SNPedia
| Orientation | plus |
| Stabilized | plus |
| Make rs6904029(A;A) |
| Make rs6904029(A;G) |
| Make rs6904029(G;G) |
| Reference | GRCh38 38.1/141 |
| Chromosome | 6 |
| Position | 29975290 |
| Gene | HCG9 |
| is a | snp |
| is | mentioned by |
| dbSNP | rs6904029 |
| dbSNP (classic) | rs6904029 |
| ClinGen | rs6904029 |
| ebi | rs6904029 |
| HLI | rs6904029 |
| Exac | rs6904029 |
| Gnomad | rs6904029 |
| Varsome | rs6904029 |
| LitVar | rs6904029 |
| Map | rs6904029 |
| PheGenI | rs6904029 |
| Biobank | rs6904029 |
| 1000 genomes | rs6904029 |
| hgdp | rs6904029 |
| ensembl | rs6904029 |
| geneview | rs6904029 |
| scholar | rs6904029 |
| rs6904029 | |
| pharmgkb | rs6904029 |
| gwascentral | rs6904029 |
| openSNP | rs6904029 |
| 23andMe | rs6904029 |
| SNPshot | rs6904029 |
| SNPdbe | rs6904029 |
| MSV3d | rs6904029 |
| GWAS Ctlg | rs6904029 |
| GMAF | 0.2842 |
| Max Magnitude | 0 |
| ? | (A;A) (A;G) (G;G) | 28 |
|---|---|---|
|
| ||
| GWAS snp | |
|---|---|
| PMID | [PMID 20410501 ]
|
| Trait | Vitiligo |
| Title | Variant of TYR and Autoimmunity Susceptibility Loci in Generalized Vitiligo |
| Risk Allele | A |
| P-val | 1E-21 |
| Odds Ratio | 1.49 [1.37-1.61] |
[PMID 22286212] Genome-Wide Association Study of Classical Hodgkin Lymphoma and Epstein-Barr Virus Status-Defined Subgroups
[PMID 19010793] Genome-wide association analysis of susceptibility and clinical phenotype in multiple sclerosis.
| GWAS snp | |
|---|---|
| PMID | [PMID 24939585]
|
| Trait | Age-related hearing impairment |
| Title | Genome-wide association analysis demonstrates the highly polygenic character of age-related hearing impairment. |
| Risk Allele | |
| P-val | 3E-6 |
| Odds Ratio | .05 [NR] unit decrease |
