Rs9811792
From SNPedia
| is a | snp |
| is | mentioned by |
| dbSNP | rs9811792 |
| hapmap | rs9811792 |
| hgdp | rs9811792 |
| ensembl | rs9811792 |
| gopubmed | rs9811792 |
| scholar | rs9811792 |
| rs9811792 | |
| pharmgkb | rs9811792 |
| hgvbaseg2p | rs9811792 |
| medrefsnp | rs9811792 |
| 23andMe | rs9811792 |
| SNP Nexus |
| Chromosome | 3 |
| Orientation | plus |
| Position | 161179691 |
| Genotype | Effect |
|---|---|
| rs9811792(C;C)* | ? |
| rs9811792(C;T)* | ? |
| rs9811792(T;T)* | ? |
Related to CELIAC DISEASE, SUSCEPTIBILITY TO, 10; CELIAC10
according to omim 612008. See also
[PMID 19693089] Four novel coeliac disease regions replicated in an association study of a Swedish-Norwegian family cohort
| ? | (C;C) (C;T) (T;T) |
|---|---|
|
| |
