rs2228055
From SNPedia
Orientation | plus |
Stabilized | plus |
Geno | Mag | Summary |
---|---|---|
(A;A) | 0 | common in clinvar |
Make rs2228055(A;G) |
Make rs2228055(G;G) |
Reference | GRCh38 38.1/141 |
Chromosome | 11 |
Position | 117994131 |
Gene | IL10RA |
is a | snp |
is | mentioned by |
dbSNP | rs2228055 |
dbSNP (classic) | rs2228055 |
ClinGen | rs2228055 |
ebi | rs2228055 |
HLI | rs2228055 |
Exac | rs2228055 |
Gnomad | rs2228055 |
Varsome | rs2228055 |
LitVar | rs2228055 |
Map | rs2228055 |
PheGenI | rs2228055 |
Biobank | rs2228055 |
1000 genomes | rs2228055 |
hgdp | rs2228055 |
ensembl | rs2228055 |
geneview | rs2228055 |
scholar | rs2228055 |
rs2228055 | |
pharmgkb | rs2228055 |
gwascentral | rs2228055 |
openSNP | rs2228055 |
23andMe | rs2228055 |
SNPshot | rs2228055 |
SNPdbe | rs2228055 |
MSV3d | rs2228055 |
GWAS Ctlg | rs2228055 |
GMAF | 0.1217 |
Max Magnitude | 0 |
[PMID 22550014] IL-10R polymorphisms are associated with very-early-onset ulcerative colitis
? | (A;A) (A;G) (G;G) | |
---|---|---|
|
[PMID 18254984] Screening of functional and positional candidate genes in families with common variable immunodeficiency.
[PMID 24081683] Evaluation of hepatitis C virus as a risk factor for HIV-associated neuroretinal disorder
ClinVar | |
---|---|
Risk | rs2228055(G;G) |
Alt | rs2228055(G;G) |
Reference | Rs2228055(A;A) |
Significance | Non-pathogenic |
Disease | Inflammatory bowel disease |
Variation | info |
Gene | IL10RA |
CLNDBN | Inflammatory bowel disease |
Reversed | 0 |
HGVS | NC_000011.9:g.117864846A>G |
CLNSRC | |
CLNACC | RCV000312221.1, |