rs1405262
From SNPedia
Orientation | plus |
Stabilized | plus |
Make rs1405262(C;C) |
Make rs1405262(C;T) |
Make rs1405262(T;T) |
Reference | GRCh38 38.1/141 |
Chromosome | 2 |
Position | 5994808 |
is a | snp |
is | mentioned by |
dbSNP | rs1405262 |
dbSNP (classic) | rs1405262 |
ClinGen | rs1405262 |
ebi | rs1405262 |
HLI | rs1405262 |
Exac | rs1405262 |
Gnomad | rs1405262 |
Varsome | rs1405262 |
LitVar | rs1405262 |
Map | rs1405262 |
PheGenI | rs1405262 |
Biobank | rs1405262 |
1000 genomes | rs1405262 |
hgdp | rs1405262 |
ensembl | rs1405262 |
geneview | rs1405262 |
scholar | rs1405262 |
rs1405262 | |
pharmgkb | rs1405262 |
gwascentral | rs1405262 |
openSNP | rs1405262 |
23andMe | rs1405262 |
SNPshot | rs1405262 |
SNPdbe | rs1405262 |
MSV3d | rs1405262 |
GWAS Ctlg | rs1405262 |
GMAF | 0.1905 |
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 | 0.000006 |
Odds Ratio | NR NR |