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rs139956886

From SNPedia

Orientationplus
Stabilizedplus
Make rs139956886(C;C)
Make rs139956886(C;T)
Make rs139956886(T;T)
ReferenceGRCh38 38.1/142
ChromosomeX
Position143759024
is asnp
is mentioned by
dbSNPrs139956886
dbSNP (old)rs139956886
ClinGenrs139956886
ebirs139956886
HLIrs139956886
Exacrs139956886
Gnomadrs139956886
Varsomers139956886
Maprs139956886
PheGenIrs139956886
Biobankrs139956886
1000 genomesrs139956886
hgdprs139956886
ensemblrs139956886
gopubmedrs139956886
geneviewrs139956886
scholarrs139956886
googlers139956886
pharmgkbrs139956886
gwascentralrs139956886
openSNPrs139956886
23andMers139956886
23andMe allrs139956886
SNP Nexus

SNPshotrs139956886
SNPdbers139956886
MSV3drs139956886
GWAS Ctlgrs139956886
Max Magnitude
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 C
P-val 6E-6
Odds Ratio 8.33 [NR]