Rs11648785
From SNPedia
| Orientation | plus |
| is a | snp |
| is | mentioned by |
| dbSNP | rs11648785 |
| PheGenI | rs11648785 |
| nextbio | rs11648785 |
| hapmap | rs11648785 |
| 1000 genomes | rs11648785 |
| hgdp | rs11648785 |
| ensembl | rs11648785 |
| gopubmed | rs11648785 |
| geneview | rs11648785 |
| scholar | rs11648785 |
| rs11648785 | |
| pharmgkb | rs11648785 |
| gwascentral | rs11648785 |
| openSNP | rs11648785 |
| 23andMe | rs11648785 |
| 23andMe all | rs11648785 |
| SNP Nexus | |
| SNPshot | rs11648785 |
| SNPdbe | rs11648785 |
| MSV3d | rs11648785 |
| Gene | DBNDD1 |
| Chromosome | 16 |
| Orientation | plus |
| GMAF | 0.2537 |
| Position | 90084561 |
| Reference | GRCh37 37.1/131 |
| Max Magnitude |
| Make rs11648785(C;C) |
| Make rs11648785(C;T) |
| Make rs11648785(T;T) |
| ? | (C;C) (C;T) (T;T) | 28 |
|---|---|---|
| GWAS snp | |
|---|---|
| PMID | [PMID 19340012] |
| Trait | Tanning |
| Title | Genome-Wide Association Study of Tanning Phenotype in a Population of European Ancestry |
| Risk Allele | T |
| P-val | 3E-9 |
| Odds Ratio | |
[PMID 20585627] Web-based, participant-driven studies yield novel genetic associations for common traits.
| GET Evidence | |
|---|---|
| rs11648785 | |
| aa_change | |
| aa_change_short | |
| impact | pathogenic |
| qualified_impact | Insufficiently evaluated pathogenic |
| overall_frequency | 0.266129 |
| summary | |
