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rs4143332

From SNPedia

Orientationminus
Make rs4143332(C;C)
Make rs4143332(C;T)
Make rs4143332(T;T)
ReferenceGRCh38.p2 38.2/144
Chromosome6
Position31380588
is asnp
is mentioned by
dbSNPrs4143332
ebirs4143332
HLIrs4143332
Exacrs4143332
Varsomers4143332
Maprs4143332
PheGenIrs4143332
hapmaprs4143332
1000 genomesrs4143332
hgdprs4143332
ensemblrs4143332
gopubmedrs4143332
geneviewrs4143332
scholarrs4143332
googlers4143332
pharmgkbrs4143332
gwascentralrs4143332
openSNPrs4143332
23andMers4143332
23andMe allrs4143332
SNP Nexus

SNPshotrs4143332
SNPdbers4143332
MSV3drs4143332
GWAS Ctlgrs4143332
Max Magnitude
? (C;C) (C;T) (T;T) 28

[PMID 26525574] Dense genotyping of immune-related loci identifies HLA variants associated with increased risk of collagenous colitis