rs264943
From SNPedia
Orientation | plus |
Stabilized | plus |
Make rs264943(A;A) |
Make rs264943(A;C) |
Make rs264943(C;C) |
Reference | GRCh38 38.1/141 |
Chromosome | 2 |
Position | 103682083 |
is a | snp |
is | mentioned by |
dbSNP | rs264943 |
dbSNP (classic) | rs264943 |
ClinGen | rs264943 |
ebi | rs264943 |
HLI | rs264943 |
Exac | rs264943 |
Gnomad | rs264943 |
Varsome | rs264943 |
LitVar | rs264943 |
Map | rs264943 |
PheGenI | rs264943 |
Biobank | rs264943 |
1000 genomes | rs264943 |
hgdp | rs264943 |
ensembl | rs264943 |
geneview | rs264943 |
scholar | rs264943 |
rs264943 | |
pharmgkb | rs264943 |
gwascentral | rs264943 |
openSNP | rs264943 |
23andMe | rs264943 |
SNPshot | rs264943 |
SNPdbe | rs264943 |
MSV3d | rs264943 |
GWAS Ctlg | rs264943 |
GMAF | 0.3104 |
Max Magnitude | 0 |
? | (A;A) (A;C) (C;C) | 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 | 0.000007 |
Odds Ratio | None None |