rs7969151
From SNPedia
Orientation | plus |
Stabilized | plus |
Make rs7969151(A;A) |
Make rs7969151(A;G) |
Make rs7969151(G;G) |
Reference | GRCh38 38.1/141 |
Chromosome | 12 |
Position | 53765493 |
is a | snp |
is | mentioned by |
dbSNP | rs7969151 |
dbSNP (classic) | rs7969151 |
ClinGen | rs7969151 |
ebi | rs7969151 |
HLI | rs7969151 |
Exac | rs7969151 |
Gnomad | rs7969151 |
Varsome | rs7969151 |
LitVar | rs7969151 |
Map | rs7969151 |
PheGenI | rs7969151 |
Biobank | rs7969151 |
1000 genomes | rs7969151 |
hgdp | rs7969151 |
ensembl | rs7969151 |
geneview | rs7969151 |
scholar | rs7969151 |
rs7969151 | |
pharmgkb | rs7969151 |
gwascentral | rs7969151 |
openSNP | rs7969151 |
23andMe | rs7969151 |
SNPshot | rs7969151 |
SNPdbe | rs7969151 |
MSV3d | rs7969151 |
GWAS Ctlg | rs7969151 |
GMAF | 0.1814 |
Max Magnitude | 0 |
? | (A;A) (A;G) (G;G) | 28 |
---|---|---|
|
GWAS snp | |
---|---|
PMID | [PMID 19340012] |
Trait | Tanning |
Title | Genome-Wide Association Study of Tanning Phenotype in a Population of European Ancestry |
Risk Allele | A |
P-val | 0.000002 |
Odds Ratio |