rs3135932

plus

Geno	Mag	Summary
(A;A)	0	common on affy axiom data

Make rs3135932(A;G)

Make rs3135932(G;G)

Reference

GRCh38 38.1/141

Chromosome

11

Position

117993348

Gene

IL10RA

is a	snp
is	mentioned by
dbSNP	rs3135932
dbSNP (classic)	rs3135932
ClinGen	rs3135932
ebi	rs3135932
HLI	rs3135932
Exac	rs3135932
Gnomad	rs3135932
Varsome	rs3135932
LitVar	rs3135932
Map	rs3135932
PheGenI	rs3135932
Biobank	rs3135932
1000 genomes	rs3135932
hgdp	rs3135932
ensembl	rs3135932
geneview	rs3135932
scholar	rs3135932
google	rs3135932
pharmgkb	rs3135932
gwascentral	rs3135932
openSNP	rs3135932
23andMe	rs3135932
SNPshot	rs3135932
SNPdbe	rs3135932
MSV3d	rs3135932
GWAS Ctlg	rs3135932

GMAF

0.08264

Max Magnitude

0

?

(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 20478055 ] Evaluation of 6 candidate genes on chromosome 11q23 for coeliac disease susceptibility: a case control study.

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

ClinVar
Risk	rs3135932(G;G)
Alt	rs3135932(G;G)
Reference	Rs3135932(A;A)
Significance	Probable-non-pathogenic
Disease	not specified Inflammatory bowel disease
Variation	info
Gene	IL10RA
CLNDBN	not specified Inflammatory bowel disease
Reversed	0
HGVS	NC_000011.9:g.117864063A>G
CLNSRC	UniProtKB (protein)
CLNACC	RCV000178165.1, RCV000356798.1,

[PMID 28225209] Association of the IL-10 receptor A536G (S138G) loss-of-function variant with multiple sclerosis in Tunisian patients.

[PMID 30594267 ] Association of a PD-L2 Gene Polymorphism with Chronic Lymphatic Filariasis in a South Indian Cohort.