rs2637496
From SNPedia
Orientation | plus |
Stabilized | plus |
Geno | Mag | Summary |
---|---|---|
(C;C) | 0 | common in complete genomics |
Make rs2637496(C;T) |
Make rs2637496(T;T) |
Reference | GRCh38 38.1/141 |
Chromosome | 5 |
Position | 125407574 |
is a | snp |
is | mentioned by |
dbSNP | rs2637496 |
dbSNP (classic) | rs2637496 |
ClinGen | rs2637496 |
ebi | rs2637496 |
HLI | rs2637496 |
Exac | rs2637496 |
Gnomad | rs2637496 |
Varsome | rs2637496 |
LitVar | rs2637496 |
Map | rs2637496 |
PheGenI | rs2637496 |
Biobank | rs2637496 |
1000 genomes | rs2637496 |
hgdp | rs2637496 |
ensembl | rs2637496 |
geneview | rs2637496 |
scholar | rs2637496 |
rs2637496 | |
pharmgkb | rs2637496 |
gwascentral | rs2637496 |
openSNP | rs2637496 |
23andMe | rs2637496 |
SNPshot | rs2637496 |
SNPdbe | rs2637496 |
MSV3d | rs2637496 |
GWAS Ctlg | rs2637496 |
GMAF | 0.1552 |
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 | 0.000009 |
Odds Ratio | NR NR |