rs7279441
From SNPedia
Orientation | plus |
Stabilized | plus |
Make rs7279441(A;A) |
Make rs7279441(A;G) |
Make rs7279441(G;G) |
Reference | GRCh38 38.1/141 |
Chromosome | 21 |
Position | 22826494 |
is a | snp |
is | mentioned by |
dbSNP | rs7279441 |
dbSNP (classic) | rs7279441 |
ClinGen | rs7279441 |
ebi | rs7279441 |
HLI | rs7279441 |
Exac | rs7279441 |
Gnomad | rs7279441 |
Varsome | rs7279441 |
LitVar | rs7279441 |
Map | rs7279441 |
PheGenI | rs7279441 |
Biobank | rs7279441 |
1000 genomes | rs7279441 |
hgdp | rs7279441 |
ensembl | rs7279441 |
geneview | rs7279441 |
scholar | rs7279441 |
rs7279441 | |
pharmgkb | rs7279441 |
gwascentral | rs7279441 |
openSNP | rs7279441 |
23andMe | rs7279441 |
SNPshot | rs7279441 |
SNPdbe | rs7279441 |
MSV3d | rs7279441 |
GWAS Ctlg | rs7279441 |
GMAF | 0.1795 |
Max Magnitude | 0 |
? | (A;A) (A;G) (G;G) | 28 |
---|---|---|
|
GWAS snp | |
---|---|
PMID | [PMID 20707712] |
Trait | |
Title | A genome-wide association study of self-rated health |
Risk Allele | G |
P-val | 0.000008 |
Odds Ratio | 0.03 [NR] unit increase |