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rs3171425

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs3171425(A;G)
Make rs3171425(G;G)
ReferenceGRCh38 38.1/141
Chromosome21
Position33296442
GeneIL10RB
is asnp
is mentioned by
dbSNPrs3171425
dbSNP (classic)rs3171425
ClinGenrs3171425
ebirs3171425
HLIrs3171425
Exacrs3171425
Gnomadrs3171425
Varsomers3171425
LitVarrs3171425
Maprs3171425
PheGenIrs3171425
Biobankrs3171425
1000 genomesrs3171425
hgdprs3171425
ensemblrs3171425
geneviewrs3171425
scholarrs3171425
googlers3171425
pharmgkbrs3171425
gwascentralrs3171425
openSNPrs3171425
23andMers3171425
SNPshotrs3171425
SNPdbers3171425
MSV3drs3171425
GWAS Ctlgrs3171425
GMAF0.4238
Max Magnitude0
? (A;A) (A;G) (G;G) 28


[PMID 21917900] Genetic Variations and Interactions in Anti-inflammatory Cytokine Pathway Genes in the Outcome of Leprosy: A Study Conducted on a MassARRAY Platform


[PMID 19230157OA-icon.png] Immunogenetics of seasonal influenza vaccine response.


ClinVar
Risk rs3171425(G;G)
Alt rs3171425(G;G)
Reference Rs3171425(A;A)
Significance Non-pathogenic
Disease Inflammatory bowel disease
Variation info
Gene IL10RB
CLNDBN Inflammatory bowel disease
Reversed 0
HGVS NC_000021.8:g.34668747A>G
CLNSRC
CLNACC RCV000270142.1,