rs6776297
From SNPedia
Orientation | plus |
Stabilized | plus |
Make rs6776297(A;A) |
Make rs6776297(A;G) |
Make rs6776297(G;G) |
Reference | GRCh38 38.1/141 |
Chromosome | 3 |
Position | 32336779 |
Gene | CMTM8 |
is a | snp |
is | mentioned by |
dbSNP | rs6776297 |
dbSNP (classic) | rs6776297 |
ClinGen | rs6776297 |
ebi | rs6776297 |
HLI | rs6776297 |
Exac | rs6776297 |
Gnomad | rs6776297 |
Varsome | rs6776297 |
LitVar | rs6776297 |
Map | rs6776297 |
PheGenI | rs6776297 |
Biobank | rs6776297 |
1000 genomes | rs6776297 |
hgdp | rs6776297 |
ensembl | rs6776297 |
geneview | rs6776297 |
scholar | rs6776297 |
rs6776297 | |
pharmgkb | rs6776297 |
gwascentral | rs6776297 |
openSNP | rs6776297 |
23andMe | rs6776297 |
SNPshot | rs6776297 |
SNPdbe | rs6776297 |
MSV3d | rs6776297 |
GWAS Ctlg | rs6776297 |
GMAF | 0.2319 |
Max Magnitude | 0 |
? | (A;A) (A;G) (G;G) | 28 |
---|---|---|
|
GWAS snp | |
---|---|
PMID | [PMID 22174851![]() |
Trait | |
Title | Genomewide association study for determinants of HIV-1 acquisition and viral set point in HIV-1 serodiscordant couples with quantified virus exposure. |
Risk Allele | |
P-val | 0.000005 |
Odds Ratio | None None |