rs13096142
From SNPedia
| Orientation | plus |
| Stabilized | plus |
| Make rs13096142(C;C) |
| Make rs13096142(C;T) |
| Make rs13096142(T;T) |
| Reference | GRCh38 38.1/142 |
| Chromosome | 3 |
| Position | 46240253 |
| Gene | CCR3 |
| is a | snp |
| is | mentioned by |
| dbSNP | rs13096142 |
| dbSNP (classic) | rs13096142 |
| ClinGen | rs13096142 |
| ebi | rs13096142 |
| HLI | rs13096142 |
| Exac | rs13096142 |
| Gnomad | rs13096142 |
| Varsome | rs13096142 |
| LitVar | rs13096142 |
| Map | rs13096142 |
| PheGenI | rs13096142 |
| Biobank | rs13096142 |
| 1000 genomes | rs13096142 |
| hgdp | rs13096142 |
| ensembl | rs13096142 |
| geneview | rs13096142 |
| scholar | rs13096142 |
| rs13096142 | |
| pharmgkb | rs13096142 |
| gwascentral | rs13096142 |
| openSNP | rs13096142 |
| 23andMe | rs13096142 |
| SNPshot | rs13096142 |
| SNPdbe | rs13096142 |
| MSV3d | rs13096142 |
| GWAS Ctlg | rs13096142 |
| Max Magnitude | 0 |
| ? | (C;C) (C;T) (T;T) | 28 |
|---|---|---|
|
| ||
| GWAS snp | |
|---|---|
| PMID | [PMID 24999842 |
| Trait | Celiac disease |
| Title | Genome-wide association study of celiac disease in North America confirms FRMD4B as new celiac locus. |
| Risk Allele | |
| P-val | 4E-8 |
| Odds Ratio | 1.30 [1.18-1.43] |
Categories:
- Is a snp
- In dbSNP
- SNPs on chromosome 3
- Has genotype
- Has population
- On chip 23andMe v1
- On chip 23andMe v2
- On chip 23andMe v3
- On chip 23andMe v4
- On chip Affy GenomeWide 6
- On chip Ancestry v2
- On chip FTDNA2
- On chip FTDNA
- On chip HumanOmni1Quad
- On chip Illumina Human 1M
- On chip 23andMe v5
- On chip Ancestry v2c
- On chip Ancestry v2d
