rs17043947
From SNPedia
Orientation | plus |
Stabilized | plus |
Make rs17043947(C;C) |
Make rs17043947(C;T) |
Make rs17043947(T;T) |
Reference | GRCh38 38.1/141 |
Chromosome | 2 |
Position | 22514115 |
Gene | LOC105374322 |
is a | snp |
is | mentioned by |
dbSNP | rs17043947 |
dbSNP (classic) | rs17043947 |
ClinGen | rs17043947 |
ebi | rs17043947 |
HLI | rs17043947 |
Exac | rs17043947 |
Gnomad | rs17043947 |
Varsome | rs17043947 |
LitVar | rs17043947 |
Map | rs17043947 |
PheGenI | rs17043947 |
Biobank | rs17043947 |
1000 genomes | rs17043947 |
hgdp | rs17043947 |
ensembl | rs17043947 |
geneview | rs17043947 |
scholar | rs17043947 |
rs17043947 | |
pharmgkb | rs17043947 |
gwascentral | rs17043947 |
openSNP | rs17043947 |
23andMe | rs17043947 |
SNPshot | rs17043947 |
SNPdbe | rs17043947 |
MSV3d | rs17043947 |
GWAS Ctlg | rs17043947 |
GMAF | 0.1102 |
Max Magnitude | 0 |
? | (C;C) (C;T) (T;T) | 28 |
---|---|---|
|
GWAS snp | |
---|---|
PMID | [PMID 20707712] |
Trait | |
Title | A genome-wide association study of self-rated health |
Risk Allele | T |
P-val | 2E-7 |
Odds Ratio | 0.07 [NR] unit decrease |