rs13076312
From SNPedia
| Orientation | plus |
| Stabilized | plus |
| Make rs13076312(C;C) |
| Make rs13076312(C;T) |
| Make rs13076312(T;T) |
| Reference | GRCh38 38.1/141 |
| Chromosome | 3 |
| Position | 188371466 |
| Gene | LPP |
| is a | snp |
| is | mentioned by |
| dbSNP | rs13076312 |
| dbSNP (classic) | rs13076312 |
| ClinGen | rs13076312 |
| ebi | rs13076312 |
| HLI | rs13076312 |
| Exac | rs13076312 |
| Gnomad | rs13076312 |
| Varsome | rs13076312 |
| LitVar | rs13076312 |
| Map | rs13076312 |
| PheGenI | rs13076312 |
| Biobank | rs13076312 |
| 1000 genomes | rs13076312 |
| hgdp | rs13076312 |
| ensembl | rs13076312 |
| geneview | rs13076312 |
| scholar | rs13076312 |
| rs13076312 | |
| pharmgkb | rs13076312 |
| gwascentral | rs13076312 |
| openSNP | rs13076312 |
| 23andMe | rs13076312 |
| SNPshot | rs13076312 |
| SNPdbe | rs13076312 |
| MSV3d | rs13076312 |
| GWAS Ctlg | rs13076312 |
| GMAF | 0.4945 |
| Max Magnitude | 0 |
| ? | (C;C) (C;T) (T;T) | 28 |
|---|---|---|
|
| ||
[PMID 18311140
] Newly identified genetic risk variants for celiac disease related to the immune response.
