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rs2057178

From SNPedia

Orientationminus
Stabilizedplus
Make rs2057178(C;C)
Make rs2057178(C;T)
Make rs2057178(T;T)
ReferenceGRCh38 38.1/142
Chromosome11
Position32342641
is asnp
is mentioned by
dbSNPrs2057178
ebirs2057178
HLIrs2057178
Exacrs2057178
Varsomers2057178
Maprs2057178
PheGenIrs2057178
hapmaprs2057178
1000 genomesrs2057178
hgdprs2057178
ensemblrs2057178
gopubmedrs2057178
geneviewrs2057178
scholarrs2057178
googlers2057178
pharmgkbrs2057178
gwascentralrs2057178
openSNPrs2057178
23andMers2057178
23andMe allrs2057178
SNP Nexus

SNPshotrs2057178
SNPdbers2057178
MSV3drs2057178
GWAS Ctlgrs2057178
GMAF0.1543
Max Magnitude
? (C;C) (C;T) (T;T) 28
[PMID 22306650OA-icon.png] Common variants at 11p13 are associated with susceptibility to tuberculosis

[PMID 23113532] Lack of association between polymorphisms from genome-wide association studies and tuberculosis in the Chinese population

GWAS snp
PMID [PMID 24057671OA-icon.png]
Trait Tuberculosis
Title Genome-wide association study of ancestry-specific TB risk in the South African Coloured population.
Risk Allele A
P-val 3E-6
Odds Ratio 1.61 [NR]