rs139956886
From SNPedia
Orientation | plus |
Stabilized | plus |
Make rs139956886(C;C) |
Make rs139956886(C;T) |
Make rs139956886(T;T) |
Reference | GRCh38 38.1/142 |
Chromosome | X |
Position | 143759024 |
is a | snp |
is | mentioned by |
dbSNP | rs139956886 |
dbSNP (classic) | rs139956886 |
ClinGen | rs139956886 |
ebi | rs139956886 |
HLI | rs139956886 |
Exac | rs139956886 |
Gnomad | rs139956886 |
Varsome | rs139956886 |
LitVar | rs139956886 |
Map | rs139956886 |
PheGenI | rs139956886 |
Biobank | rs139956886 |
1000 genomes | rs139956886 |
hgdp | rs139956886 |
ensembl | rs139956886 |
geneview | rs139956886 |
scholar | rs139956886 |
rs139956886 | |
pharmgkb | rs139956886 |
gwascentral | rs139956886 |
openSNP | rs139956886 |
23andMe | rs139956886 |
SNPshot | rs139956886 |
SNPdbe | rs139956886 |
MSV3d | rs139956886 |
GWAS Ctlg | rs139956886 |
Max Magnitude | 0 |
GWAS snp | |
---|---|
PMID | [PMID 24057671] |
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] |