rs17025867
From SNPedia
Orientation | plus |
Stabilized | plus |
Geno | Mag | Summary |
---|---|---|
(G;G) | 0 | common genotype |
Make rs17025867(A;A) |
Make rs17025867(A;G) |
Reference | GRCh38 38.1/141 |
Chromosome | 2 |
Position | 40351419 |
Gene | SLC8A1 |
is a | snp |
is | mentioned by |
dbSNP | rs17025867 |
dbSNP (classic) | rs17025867 |
ClinGen | rs17025867 |
ebi | rs17025867 |
HLI | rs17025867 |
Exac | rs17025867 |
Gnomad | rs17025867 |
Varsome | rs17025867 |
LitVar | rs17025867 |
Map | rs17025867 |
PheGenI | rs17025867 |
Biobank | rs17025867 |
1000 genomes | rs17025867 |
hgdp | rs17025867 |
ensembl | rs17025867 |
geneview | rs17025867 |
scholar | rs17025867 |
rs17025867 | |
pharmgkb | rs17025867 |
gwascentral | rs17025867 |
openSNP | rs17025867 |
23andMe | rs17025867 |
SNPshot | rs17025867 |
SNPdbe | rs17025867 |
MSV3d | rs17025867 |
GWAS Ctlg | rs17025867 |
GMAF | 0.007346 |
Max Magnitude | 0 |
? | (A;A) (A;G) (G;G) | 28 |
---|---|---|
|
GWAS snp | |
---|---|
PMID | [PMID 23563609] |
Trait | Obesity (early onset extreme) |
Title | Genome-wide SNP and CNV analysis identifies common and low-frequency variants associated with severe early-onset obesity. |
Risk Allele | A |
P-val | 2E-7 |
Odds Ratio | 1.81 [1.45-2.27] |