rs9367630
From SNPedia
Orientation | plus |
Stabilized | plus |
Geno | Mag | Summary |
---|---|---|
(G;G) | 0 | common in complete genomics |
Make rs9367630(A;A) |
Make rs9367630(A;G) |
Reference | GRCh38 38.1/141 |
Chromosome | 6 |
Position | 55283305 |
Gene | HCRTR2 |
is a | snp |
is | mentioned by |
dbSNP | rs9367630 |
dbSNP (classic) | rs9367630 |
ClinGen | rs9367630 |
ebi | rs9367630 |
HLI | rs9367630 |
Exac | rs9367630 |
Gnomad | rs9367630 |
Varsome | rs9367630 |
LitVar | rs9367630 |
Map | rs9367630 |
PheGenI | rs9367630 |
Biobank | rs9367630 |
1000 genomes | rs9367630 |
hgdp | rs9367630 |
ensembl | rs9367630 |
geneview | rs9367630 |
scholar | rs9367630 |
rs9367630 | |
pharmgkb | rs9367630 |
gwascentral | rs9367630 |
openSNP | rs9367630 |
23andMe | rs9367630 |
SNPshot | rs9367630 |
SNPdbe | rs9367630 |
MSV3d | rs9367630 |
GWAS Ctlg | rs9367630 |
GMAF | 0.1194 |
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 | 1E-7 |
Odds Ratio | NR NR |