rs9328321
From SNPedia
Orientation | plus |
Stabilized | plus |
Make rs9328321(A;A) |
Make rs9328321(A;G) |
Make rs9328321(G;G) |
Reference | GRCh38 38.1/141 |
Chromosome | 6 |
Position | 5600205 |
Gene | FARS2 |
is a | snp |
is | mentioned by |
dbSNP | rs9328321 |
dbSNP (classic) | rs9328321 |
ClinGen | rs9328321 |
ebi | rs9328321 |
HLI | rs9328321 |
Exac | rs9328321 |
Gnomad | rs9328321 |
Varsome | rs9328321 |
LitVar | rs9328321 |
Map | rs9328321 |
PheGenI | rs9328321 |
Biobank | rs9328321 |
1000 genomes | rs9328321 |
hgdp | rs9328321 |
ensembl | rs9328321 |
geneview | rs9328321 |
scholar | rs9328321 |
rs9328321 | |
pharmgkb | rs9328321 |
gwascentral | rs9328321 |
openSNP | rs9328321 |
23andMe | rs9328321 |
SNPshot | rs9328321 |
SNPdbe | rs9328321 |
MSV3d | rs9328321 |
GWAS Ctlg | rs9328321 |
GMAF | 0.2989 |
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 | 5E-7 |
Odds Ratio | 1.22 [1.13-1.32] |