rs13111989
From SNPedia
Orientation | plus |
Stabilized | plus |
Make rs13111989(A;A) |
Make rs13111989(A;G) |
Make rs13111989(G;G) |
Reference | GRCh38 38.1/141 |
Chromosome | 4 |
Position | 176621822 |
is a | snp |
is | mentioned by |
dbSNP | rs13111989 |
dbSNP (classic) | rs13111989 |
ClinGen | rs13111989 |
ebi | rs13111989 |
HLI | rs13111989 |
Exac | rs13111989 |
Gnomad | rs13111989 |
Varsome | rs13111989 |
LitVar | rs13111989 |
Map | rs13111989 |
PheGenI | rs13111989 |
Biobank | rs13111989 |
1000 genomes | rs13111989 |
hgdp | rs13111989 |
ensembl | rs13111989 |
geneview | rs13111989 |
scholar | rs13111989 |
rs13111989 | |
pharmgkb | rs13111989 |
gwascentral | rs13111989 |
openSNP | rs13111989 |
23andMe | rs13111989 |
SNPshot | rs13111989 |
SNPdbe | rs13111989 |
MSV3d | rs13111989 |
GWAS Ctlg | rs13111989 |
GMAF | 0.1846 |
Max Magnitude | 0 |
? | (A;A) (A;G) (G;G) | 28 |
---|---|---|
|
GWAS snp | |
---|---|
PMID | [PMID 22174851] |
Trait | |
Title | Genomewide association study for determinants of HIV-1 acquisition and viral set point in HIV-1 serodiscordant couples with quantified virus exposure. |
Risk Allele | |
P-val | 2E-7 |
Odds Ratio | None None |