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rs6421571

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in complete genomics
Make rs6421571(C;T)
Make rs6421571(T;T)
ReferenceGRCh38 38.1/141
Chromosome11
Position118873063
is asnp
is mentioned by
dbSNPrs6421571
ebirs6421571
HLIrs6421571
Exacrs6421571
Varsomers6421571
Maprs6421571
PheGenIrs6421571
hapmaprs6421571
1000 genomesrs6421571
hgdprs6421571
ensemblrs6421571
gopubmedrs6421571
geneviewrs6421571
scholarrs6421571
googlers6421571
pharmgkbrs6421571
gwascentralrs6421571
openSNPrs6421571
23andMers6421571
23andMe allrs6421571
SNP Nexus

SNPshotrs6421571
SNPdbers6421571
MSV3drs6421571
GWAS Ctlgrs6421571
GMAF0.1722
Max Magnitude0
? (C;C) (C;T) (T;T) 28
GWAS snp
PMID [PMID 21399635OA-icon.png]
Trait
Title Genome-wide association study identifies 12 new susceptibility loci for primary biliary cirrhosis
Risk Allele C
P-val 3E-12
Odds Ratio 1.3700 [1.25-1.50]


[PMID 22707196] C-X-C chemokine receptor type 5 gene polymorphisms are associated with non-Hodgkin lymphoma.


[PMID 24833093] C-X-C chemokine receptor type 5 gene polymorphism affects gene expression in CD4+ T cells and is associated with increased risk of colorectal cancer