rs7674482
From SNPedia
Orientation | plus |
Stabilized | plus |
Make rs7674482(C;C) |
Make rs7674482(C;T) |
Make rs7674482(T;T) |
Reference | GRCh38 38.1/141 |
Chromosome | 4 |
Position | 45865444 |
is a | snp |
is | mentioned by |
dbSNP | rs7674482 |
dbSNP (classic) | rs7674482 |
ClinGen | rs7674482 |
ebi | rs7674482 |
HLI | rs7674482 |
Exac | rs7674482 |
Gnomad | rs7674482 |
Varsome | rs7674482 |
LitVar | rs7674482 |
Map | rs7674482 |
PheGenI | rs7674482 |
Biobank | rs7674482 |
1000 genomes | rs7674482 |
hgdp | rs7674482 |
ensembl | rs7674482 |
geneview | rs7674482 |
scholar | rs7674482 |
rs7674482 | |
pharmgkb | rs7674482 |
gwascentral | rs7674482 |
openSNP | rs7674482 |
23andMe | rs7674482 |
SNPshot | rs7674482 |
SNPdbe | rs7674482 |
MSV3d | rs7674482 |
GWAS Ctlg | rs7674482 |
GMAF | 0.2801 |
Max Magnitude | 0 |
? | (C;C) (C;T) (T;T) | 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 | 0.000005 |
Odds Ratio | None None |