rs12727642
From SNPedia
| Orientation | plus |
| Stabilized | plus |
| Make rs12727642(A;A) |
| Make rs12727642(A;C) |
| Make rs12727642(C;C) |
| Reference | GRCh38 38.1/141 |
| Chromosome | 1 |
| Position | 7986612 |
| Gene | PARK7 |
| is a | snp |
| is | mentioned by |
| dbSNP | rs12727642 |
| dbSNP (classic) | rs12727642 |
| ClinGen | rs12727642 |
| ebi | rs12727642 |
| HLI | rs12727642 |
| Exac | rs12727642 |
| Gnomad | rs12727642 |
| Varsome | rs12727642 |
| LitVar | rs12727642 |
| Map | rs12727642 |
| PheGenI | rs12727642 |
| Biobank | rs12727642 |
| 1000 genomes | rs12727642 |
| hgdp | rs12727642 |
| ensembl | rs12727642 |
| geneview | rs12727642 |
| scholar | rs12727642 |
| rs12727642 | |
| pharmgkb | rs12727642 |
| gwascentral | rs12727642 |
| openSNP | rs12727642 |
| 23andMe | rs12727642 |
| SNPshot | rs12727642 |
| SNPdbe | rs12727642 |
| MSV3d | rs12727642 |
| GWAS Ctlg | rs12727642 |
| GMAF | 0.09734 |
| Max Magnitude | 0 |
| ? | (A;A) (A;C) (C;C) | 28 |
|---|---|---|
|
| ||
| GWAS snp | |
|---|---|
| PMID | [PMID 20190752 |
| Trait | Celiac disease |
| Title | Multiple common variants for celiac disease influencing immune gene expression |
| Risk Allele | A |
| P-val | 9E-8 |
| Odds Ratio | 1.14 [1.09-1.20] |
[PMID 24871462] Coeliac disease-associated polymorphisms influence thymic gene expression
