rs1463132
From SNPedia
Orientation | minus |
Stabilized | minus |
Make rs1463132(A;A) |
Make rs1463132(A;G) |
Make rs1463132(G;G) |
Reference | GRCh38 38.1/141 |
Chromosome | 16 |
Position | 10089230 |
Gene | GRIN2A |
is a | snp |
is | mentioned by |
dbSNP | rs1463132 |
dbSNP (classic) | rs1463132 |
ClinGen | rs1463132 |
ebi | rs1463132 |
HLI | rs1463132 |
Exac | rs1463132 |
Gnomad | rs1463132 |
Varsome | rs1463132 |
LitVar | rs1463132 |
Map | rs1463132 |
PheGenI | rs1463132 |
Biobank | rs1463132 |
1000 genomes | rs1463132 |
hgdp | rs1463132 |
ensembl | rs1463132 |
geneview | rs1463132 |
scholar | rs1463132 |
rs1463132 | |
pharmgkb | rs1463132 |
gwascentral | rs1463132 |
openSNP | rs1463132 |
23andMe | rs1463132 |
SNPshot | rs1463132 |
SNPdbe | rs1463132 |
MSV3d | rs1463132 |
GWAS Ctlg | rs1463132 |
GMAF | 0.3333 |
Max Magnitude | 0 |
? | (A;A) (A;G) (G;G) | 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 | 0.000008 |
Odds Ratio | NR NR |