rs7194886
From SNPedia
Orientation | plus |
Stabilized | plus |
Make rs7194886(C;C) |
Make rs7194886(C;T) |
Make rs7194886(T;T) |
Reference | GRCh38 38.1/141 |
Chromosome | 16 |
Position | 50691282 |
is a | snp |
is | mentioned by |
dbSNP | rs7194886 |
dbSNP (classic) | rs7194886 |
ClinGen | rs7194886 |
ebi | rs7194886 |
HLI | rs7194886 |
Exac | rs7194886 |
Gnomad | rs7194886 |
Varsome | rs7194886 |
LitVar | rs7194886 |
Map | rs7194886 |
PheGenI | rs7194886 |
Biobank | rs7194886 |
1000 genomes | rs7194886 |
hgdp | rs7194886 |
ensembl | rs7194886 |
geneview | rs7194886 |
scholar | rs7194886 |
rs7194886 | |
pharmgkb | rs7194886 |
gwascentral | rs7194886 |
openSNP | rs7194886 |
23andMe | rs7194886 |
SNPshot | rs7194886 |
SNPdbe | rs7194886 |
MSV3d | rs7194886 |
GWAS Ctlg | rs7194886 |
GMAF | 0.2801 |
Max Magnitude | 0 |
? | (C;C) (C;T) (T;T) | 28 |
---|---|---|
|
[PMID 22212192] Polymorphisms of NOD2 and the risk of tuberculosis: a validation study in the Chinese population
[PMID 17068223] A genome-wide association study identifies IL23R as an inflammatory bowel disease gene.
[PMID 24298015] The Role of NOD2 in Murine and Human Melioidosis