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rs13192471

From SNPedia

Orientationplus
Stabilizedplus
Make rs13192471(C;C)
Make rs13192471(C;T)
Make rs13192471(T;T)
ReferenceGRCh38 38.1/141
Chromosome6
Position32703326
is asnp
is mentioned by
dbSNPrs13192471
ebirs13192471
HLIrs13192471
Exacrs13192471
Varsomers13192471
Maprs13192471
PheGenIrs13192471
hapmaprs13192471
1000 genomesrs13192471
hgdprs13192471
ensemblrs13192471
gopubmedrs13192471
geneviewrs13192471
scholarrs13192471
googlers13192471
pharmgkbrs13192471
gwascentralrs13192471
openSNPrs13192471
23andMers13192471
23andMe allrs13192471
SNP Nexus

SNPshotrs13192471
SNPdbers13192471
MSV3drs13192471
GWAS Ctlgrs13192471
GMAF0.1988
Max Magnitude
? (C;C) (C;T) (T;T) 28
GWAS snp
PMID [PMID 20453841]
Trait Rheumatoid arthritis
Title A regulatory variant in CCR6 is associated with rheumatoid arthritis susceptibility
Risk Allele G
P-val 2E-58
Odds Ratio 1.97 [1.82-2.14]


[PMID 22355377OA-icon.png] Caucasian and asian specific rheumatoid arthritis risk Loci reveal limited replication and apparent allelic heterogeneity in north indians