rs424232
From SNPedia
| Orientation | minus |
| Stabilized | minus |
| Make rs424232(A;A) |
| Make rs424232(A;G) |
| Make rs424232(G;G) |
| Reference | GRCh38 38.1/141 |
| Chromosome | 6 |
| Position | 32240547 |
| is a | snp |
| is | mentioned by |
| dbSNP | rs424232 |
| dbSNP (classic) | rs424232 |
| ClinGen | rs424232 |
| ebi | rs424232 |
| HLI | rs424232 |
| Exac | rs424232 |
| Gnomad | rs424232 |
| Varsome | rs424232 |
| LitVar | rs424232 |
| Map | rs424232 |
| PheGenI | rs424232 |
| Biobank | rs424232 |
| 1000 genomes | rs424232 |
| hgdp | rs424232 |
| ensembl | rs424232 |
| geneview | rs424232 |
| scholar | rs424232 |
| rs424232 | |
| pharmgkb | rs424232 |
| gwascentral | rs424232 |
| openSNP | rs424232 |
| 23andMe | rs424232 |
| SNPshot | rs424232 |
| SNPdbe | rs424232 |
| MSV3d | rs424232 |
| GWAS Ctlg | rs424232 |
| GMAF | 0.2961 |
| Max Magnitude | 0 |
| ? | (A;A) (A;G) (G;G) | 28 |
|---|---|---|
|
| ||
[PMID 23053058] Search for schizophrenia susceptibility variants at the HLA-DRB1 locus among a British population
| GWAS snp | |
|---|---|
| PMID | [PMID 23936387 |
| Trait | Celiac disease |
| Title | A possible mechanism behind autoimmune disorders discovered by genome-wide linkage and association analysis in celiac disease. |
| Risk Allele | C |
| P-val | 5E-21 |
| Odds Ratio | NR NR |
Categories:
- Is a snp
- In dbSNP
- SNPs on chromosome 6
- 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
