rs9921255
From SNPedia
Orientation | plus |
Stabilized | plus |
Make rs9921255(C;C) |
Make rs9921255(C;T) |
Make rs9921255(T;T) |
Reference | GRCh38 38.1/141 |
Chromosome | 16 |
Position | 53975416 |
Gene | FTO |
is a | snp |
is | mentioned by |
dbSNP | rs9921255 |
dbSNP (classic) | rs9921255 |
ClinGen | rs9921255 |
ebi | rs9921255 |
HLI | rs9921255 |
Exac | rs9921255 |
Gnomad | rs9921255 |
Varsome | rs9921255 |
LitVar | rs9921255 |
Map | rs9921255 |
PheGenI | rs9921255 |
Biobank | rs9921255 |
1000 genomes | rs9921255 |
hgdp | rs9921255 |
ensembl | rs9921255 |
geneview | rs9921255 |
scholar | rs9921255 |
rs9921255 | |
pharmgkb | rs9921255 |
gwascentral | rs9921255 |
openSNP | rs9921255 |
23andMe | rs9921255 |
SNPshot | rs9921255 |
SNPdbe | rs9921255 |
MSV3d | rs9921255 |
GWAS Ctlg | rs9921255 |
GMAF | 0.1878 |
Max Magnitude | 0 |
? | (C;C) (C;T) (T;T) | 28 |
---|---|---|
|
[PMID 22030988] FTO Risk Haplotype Among Early Onset and Severe Obesity Cases in a Population of Western Spain