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rs2228055

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs2228055(A;G)
Make rs2228055(G;G)
ReferenceGRCh38 38.1/141
Chromosome11
Position117994131
GeneIL10RA
is asnp
is mentioned by
dbSNPrs2228055
dbSNP (old)rs2228055
ClinGenrs2228055
ebirs2228055
HLIrs2228055
Exacrs2228055
Varsomers2228055
Maprs2228055
PheGenIrs2228055
Biobankrs2228055
1000 genomesrs2228055
hgdprs2228055
ensemblrs2228055
gopubmedrs2228055
geneviewrs2228055
scholarrs2228055
googlers2228055
pharmgkbrs2228055
gwascentralrs2228055
openSNPrs2228055
23andMers2228055
23andMe allrs2228055
SNP Nexus

SNPshotrs2228055
SNPdbers2228055
MSV3drs2228055
GWAS Ctlgrs2228055
GMAF0.1217
Max Magnitude0

[PMID 22550014OA-icon.png] IL-10R polymorphisms are associated with very-early-onset ulcerative colitis

? (A;A) (A;G) (G;G)
[PMID 18254984OA-icon.png] Screening of functional and positional candidate genes in families with common variable immunodeficiency.

[PMID 24081683OA-icon.png] 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,