rs1900442
From SNPedia
Orientation | plus |
Stabilized | plus |
Make rs1900442(C;C) |
Make rs1900442(C;T) |
Make rs1900442(T;T) |
Reference | GRCh38 38.1/142 |
Chromosome | 13 |
Position | 41931538 |
Gene | VWA8 |
is a | snp |
is | mentioned by |
dbSNP | rs1900442 |
dbSNP (classic) | rs1900442 |
ClinGen | rs1900442 |
ebi | rs1900442 |
HLI | rs1900442 |
Exac | rs1900442 |
Gnomad | rs1900442 |
Varsome | rs1900442 |
LitVar | rs1900442 |
Map | rs1900442 |
PheGenI | rs1900442 |
Biobank | rs1900442 |
1000 genomes | rs1900442 |
hgdp | rs1900442 |
ensembl | rs1900442 |
geneview | rs1900442 |
scholar | rs1900442 |
rs1900442 | |
pharmgkb | rs1900442 |
gwascentral | rs1900442 |
openSNP | rs1900442 |
23andMe | rs1900442 |
SNPshot | rs1900442 |
SNPdbe | rs1900442 |
MSV3d | rs1900442 |
GWAS Ctlg | rs1900442 |
Max Magnitude | 0 |
? | (C;C) (C;T) (T;T) | 28 |
---|---|---|
|
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 | T |
P-val | 5E-6 |
Odds Ratio | 2.70 [NR] |