rs2357266
From SNPedia
Orientation | minus |
Stabilized | minus |
Make rs2357266(C;C) |
Make rs2357266(C;T) |
Make rs2357266(T;T) |
Reference | GRCh38 38.1/141 |
Chromosome | 2 |
Position | 9784258 |
is a | snp |
is | mentioned by |
dbSNP | rs2357266 |
dbSNP (classic) | rs2357266 |
ClinGen | rs2357266 |
ebi | rs2357266 |
HLI | rs2357266 |
Exac | rs2357266 |
Gnomad | rs2357266 |
Varsome | rs2357266 |
LitVar | rs2357266 |
Map | rs2357266 |
PheGenI | rs2357266 |
Biobank | rs2357266 |
1000 genomes | rs2357266 |
hgdp | rs2357266 |
ensembl | rs2357266 |
geneview | rs2357266 |
scholar | rs2357266 |
rs2357266 | |
pharmgkb | rs2357266 |
gwascentral | rs2357266 |
openSNP | rs2357266 |
23andMe | rs2357266 |
SNPshot | rs2357266 |
SNPdbe | rs2357266 |
MSV3d | rs2357266 |
GWAS Ctlg | rs2357266 |
GMAF | 0.3531 |
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 | G |
P-val | 0.000004 |
Odds Ratio | 0.02 [NR] unit decrease |