rs1120787
From SNPedia
Orientation | plus |
Stabilized | plus |
Make rs1120787(G;G) |
Make rs1120787(G;T) |
Make rs1120787(T;T) |
Reference | GRCh38 38.1/141 |
Chromosome | 18 |
Position | 57316323 |
is a | snp |
is | mentioned by |
dbSNP | rs1120787 |
dbSNP (classic) | rs1120787 |
ClinGen | rs1120787 |
ebi | rs1120787 |
HLI | rs1120787 |
Exac | rs1120787 |
Gnomad | rs1120787 |
Varsome | rs1120787 |
LitVar | rs1120787 |
Map | rs1120787 |
PheGenI | rs1120787 |
Biobank | rs1120787 |
1000 genomes | rs1120787 |
hgdp | rs1120787 |
ensembl | rs1120787 |
geneview | rs1120787 |
scholar | rs1120787 |
rs1120787 | |
pharmgkb | rs1120787 |
gwascentral | rs1120787 |
openSNP | rs1120787 |
23andMe | rs1120787 |
SNPshot | rs1120787 |
SNPdbe | rs1120787 |
MSV3d | rs1120787 |
GWAS Ctlg | rs1120787 |
GMAF | 0.1529 |
Max Magnitude | 0 |
? | (G;G) (G;T) (T;T) | 28 |
---|---|---|
|
GWAS snp | |
---|---|
PMID | [PMID 20041166] |
Trait | HIV-1 control |
Title | Common Genetic Variation and the Control of HIV-1 in Human |
Risk Allele | |
P-val | 0.000007 |
Odds Ratio | NR NR |