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