rs6544997
From SNPedia
| Orientation | plus |
| Stabilized | plus |
| Make rs6544997(A;A) |
| Make rs6544997(A;G) |
| Make rs6544997(G;G) |
| Reference | GRCh38 38.1/141 |
| Chromosome | 2 |
| Position | 47617366 |
| Gene | MSH2 |
| is a | snp |
| is | mentioned by |
| dbSNP | rs6544997 |
| dbSNP (classic) | rs6544997 |
| ClinGen | rs6544997 |
| ebi | rs6544997 |
| HLI | rs6544997 |
| Exac | rs6544997 |
| Gnomad | rs6544997 |
| Varsome | rs6544997 |
| LitVar | rs6544997 |
| Map | rs6544997 |
| PheGenI | rs6544997 |
| Biobank | rs6544997 |
| 1000 genomes | rs6544997 |
| hgdp | rs6544997 |
| ensembl | rs6544997 |
| geneview | rs6544997 |
| scholar | rs6544997 |
| rs6544997 | |
| pharmgkb | rs6544997 |
| gwascentral | rs6544997 |
| openSNP | rs6544997 |
| 23andMe | rs6544997 |
| SNPshot | rs6544997 |
| SNPdbe | rs6544997 |
| MSV3d | rs6544997 |
| GWAS Ctlg | rs6544997 |
| GMAF | 0.45 |
| Max Magnitude | 0 |
| ? | (A;A) (A;G) (G;G) | 28 |
|---|---|---|
|
| ||
| GWAS snp | |
|---|---|
| PMID | [PMID 19890347 ]
|
| Trait | Vitiligo |
| Title | Genome-Wide Association Study of Generalized Vitiligo in an Isolated European Founder Population Identifies SMOC2, in Close Proximity to IDDM8 |
| Risk Allele | |
| P-val | 0.000007 |
| Odds Ratio | NR NR |
