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rs3135932

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(A;A) 0 common on affy axiom data
Make rs3135932(A;G)
Make rs3135932(G;G)
ReferenceGRCh38 38.1/141
Chromosome11
Position117993348
GeneIL10RA
is asnp
is mentioned by
dbSNPrs3135932
ebirs3135932
HLIrs3135932
Exacrs3135932
Varsomers3135932
Maprs3135932
PheGenIrs3135932
hapmaprs3135932
1000 genomesrs3135932
hgdprs3135932
ensemblrs3135932
gopubmedrs3135932
geneviewrs3135932
scholarrs3135932
googlers3135932
pharmgkbrs3135932
gwascentralrs3135932
openSNPrs3135932
23andMers3135932
23andMe allrs3135932
SNP Nexus

SNPshotrs3135932
SNPdbers3135932
MSV3drs3135932
GWAS Ctlgrs3135932
GMAF0.08264
Max Magnitude0
? (A;A) (A;G) (G;G) 28

[PMID 21553229] IL-10R1 S138G loss-of-function polymorphism is associated with extrapulmonary tuberculosis risk development in Tunisia


[PMID 20478055OA-icon.png] Evaluation of 6 candidate genes on chromosome 11q23 for coeliac disease susceptibility: a case control study.


[PMID 20811626OA-icon.png] Genetic variants in inflammation-related genes are associated with radiation-induced toxicity following treatment for non-small cell lung cancer.


GET Evidence
IL10RA-S159G
aa_change Ser159Gly
aa_change_short S159G
impact not reviewed
qualified_impact Insufficiently evaluated not reviewed
overall_frequency 0.120097
summary



ClinVar
Risk rs3135932(G;G)
Alt rs3135932(G;G)
Reference rs3135932(A;A)
Significance Non-pathogenic
Disease not specified
Variation info
Gene IL10RA
CLNDBN not specified
Reversed 0
HGVS NC_000011.9:g.117864063A>G
CLNSRC
CLNACC RCV000178165.1,