rs9811792
From SNPedia
| Orientation | plus |
| Stabilized | plus |
| Make rs9811792(C;C) |
| Make rs9811792(C;T) |
| Make rs9811792(T;T) |
| Reference | GRCh38 38.1/141 |
| Chromosome | 3 |
| Position | 159979210 |
| Gene | IL12A-AS1 |
| is a | snp |
| is | mentioned by |
| dbSNP | rs9811792 |
| dbSNP (classic) | rs9811792 |
| ClinGen | rs9811792 |
| ebi | rs9811792 |
| HLI | rs9811792 |
| Exac | rs9811792 |
| Gnomad | rs9811792 |
| Varsome | rs9811792 |
| LitVar | rs9811792 |
| Map | rs9811792 |
| PheGenI | rs9811792 |
| Biobank | rs9811792 |
| 1000 genomes | rs9811792 |
| hgdp | rs9811792 |
| ensembl | rs9811792 |
| geneview | rs9811792 |
| scholar | rs9811792 |
| rs9811792 | |
| pharmgkb | rs9811792 |
| gwascentral | rs9811792 |
| openSNP | rs9811792 |
| 23andMe | rs9811792 |
| SNPshot | rs9811792 |
| SNPdbe | rs9811792 |
| MSV3d | rs9811792 |
| GWAS Ctlg | rs9811792 |
| GMAF | 0.4601 |
| Max Magnitude | 0 |
| ? | (C;C) (C;T) (T;T) | 28 |
|---|---|---|
|
| ||
[PMID 19693089] Four novel coeliac disease regions replicated in an association study of a Swedish-Norwegian family cohort
[PMID 22087237
] Improving the estimation of celiac disease sibling risk by non-HLA genes
[PMID 18311140] Newly identified genetic risk variants for celiac disease related to the immune response.
[PMID 19073967] Shared and distinct genetic variants in type 1 diabetes and celiac disease.
Categories:
- Is a snp
- In dbSNP
- SNPs on chromosome 3
- Has genotype
- Has population
- Uses omim
- 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
