rs7190053
From SNPedia
Orientation | plus |
Stabilized | plus |
Make rs7190053(C;C) |
Make rs7190053(C;T) |
Make rs7190053(T;T) |
Reference | GRCh38 38.1/141 |
Chromosome | 16 |
Position | 53840745 |
Gene | FTO |
is a | snp |
is | mentioned by |
dbSNP | rs7190053 |
dbSNP (classic) | rs7190053 |
ClinGen | rs7190053 |
ebi | rs7190053 |
HLI | rs7190053 |
Exac | rs7190053 |
Gnomad | rs7190053 |
Varsome | rs7190053 |
LitVar | rs7190053 |
Map | rs7190053 |
PheGenI | rs7190053 |
Biobank | rs7190053 |
1000 genomes | rs7190053 |
hgdp | rs7190053 |
ensembl | rs7190053 |
geneview | rs7190053 |
scholar | rs7190053 |
rs7190053 | |
pharmgkb | rs7190053 |
gwascentral | rs7190053 |
openSNP | rs7190053 |
23andMe | rs7190053 |
SNPshot | rs7190053 |
SNPdbe | rs7190053 |
MSV3d | rs7190053 |
GWAS Ctlg | rs7190053 |
GMAF | 0.1171 |
Max Magnitude | 0 |
? | (C;C) (C;T) (T;T) | 28 |
---|---|---|
|
[PMID 24289790] Influence of FTO variants on obesity, inflammation and cardiovascular disease risk biomarkers in Spanish children: a case--control multicentre study