rs4838508
From SNPedia
Orientation | plus |
Stabilized | plus |
Geno | Mag | Summary |
---|---|---|
(C;C) | 0 | common in complete genomics |
Make rs4838508(C;T) |
Make rs4838508(T;T) |
Reference | GRCh38 38.1/142 |
Chromosome | 10 |
Position | 49353462 |
is a | snp |
is | mentioned by |
dbSNP | rs4838508 |
dbSNP (classic) | rs4838508 |
ClinGen | rs4838508 |
ebi | rs4838508 |
HLI | rs4838508 |
Exac | rs4838508 |
Gnomad | rs4838508 |
Varsome | rs4838508 |
LitVar | rs4838508 |
Map | rs4838508 |
PheGenI | rs4838508 |
Biobank | rs4838508 |
1000 genomes | rs4838508 |
hgdp | rs4838508 |
ensembl | rs4838508 |
geneview | rs4838508 |
scholar | rs4838508 |
rs4838508 | |
pharmgkb | rs4838508 |
gwascentral | rs4838508 |
openSNP | rs4838508 |
23andMe | rs4838508 |
SNPshot | rs4838508 |
SNPdbe | rs4838508 |
MSV3d | rs4838508 |
GWAS Ctlg | rs4838508 |
GMAF | 0.03627 |
Max Magnitude | 0 |
? | (C;C) (C;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 | 0.000002 |
Odds Ratio | NR NR |