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rs6441961

From SNPedia

Orientationplus
Stabilizedplus
Make rs6441961(C;C)
Make rs6441961(C;T)
Make rs6441961(T;T)
ReferenceGRCh38 38.1/141
Chromosome3
Position46310893
GeneLOC100131327, CCR3
is asnp
is mentioned by
dbSNPrs6441961
ebirs6441961
HLIrs6441961
Exacrs6441961
Varsomers6441961
Maprs6441961
PheGenIrs6441961
hapmaprs6441961
1000 genomesrs6441961
hgdprs6441961
ensemblrs6441961
gopubmedrs6441961
geneviewrs6441961
scholarrs6441961
googlers6441961
pharmgkbrs6441961
gwascentralrs6441961
openSNPrs6441961
23andMers6441961
23andMe allrs6441961
SNP Nexus

SNPshotrs6441961
SNPdbers6441961
MSV3drs6441961
GWAS Ctlgrs6441961
GMAF0.2718
Max Magnitude
? (C;C) (C;T) (T;T) 28
GWAS snp
PMID [PMID 18311140OA-icon.png]
Trait Celiac disease
Title Newly identified genetic risk variants for celiac disease related to the immune response
Risk Allele A
P-val 2.9999999999999999E-7
Odds Ratio 1.21 [1.13-1.30]
OMIM612007
DescCELIAC DISEASE, SUSCEPTIBILITY TO, 9; CELIAC9
Variant
Relatedalso

[PMID 19693089] Four novel coeliac disease regions replicated in an association study of a Swedish-Norwegian family cohort

[PMID 19542083] Association of IL18RAP and CCR3 with coeliac disease in the Spanish population


[PMID 22087237OA-icon.png] Improving the estimation of celiac disease sibling risk by non-HLA genes

[PMID 18713140OA-icon.png] Translational mini-review series on the immunogenetics of gut disease: immunogenetics of coeliac disease.

[PMID 19073967OA-icon.png] Shared and distinct genetic variants in type 1 diabetes and celiac disease.

[PMID 20369022OA-icon.png] Candidate causal regulatory effects by integration of expression QTLs with complex trait genetic associations.


GET Evidence
rs6441961
aa_change
aa_change_short
impact pathogenic
qualified_impact Insufficiently evaluated pathogenic
overall_frequency 0.757812
summary