rs11075997
From SNPedia
Orientation | plus |
Stabilized | plus |
Make rs11075997(C;C) |
Make rs11075997(C;T) |
Make rs11075997(T;T) |
Reference | GRCh38 38.1/141 |
Chromosome | 16 |
Position | 53825000 |
Gene | FTO |
is a | snp |
is | mentioned by |
dbSNP | rs11075997 |
dbSNP (classic) | rs11075997 |
ClinGen | rs11075997 |
ebi | rs11075997 |
HLI | rs11075997 |
Exac | rs11075997 |
Gnomad | rs11075997 |
Varsome | rs11075997 |
LitVar | rs11075997 |
Map | rs11075997 |
PheGenI | rs11075997 |
Biobank | rs11075997 |
1000 genomes | rs11075997 |
hgdp | rs11075997 |
ensembl | rs11075997 |
geneview | rs11075997 |
scholar | rs11075997 |
rs11075997 | |
pharmgkb | rs11075997 |
gwascentral | rs11075997 |
openSNP | rs11075997 |
23andMe | rs11075997 |
SNPshot | rs11075997 |
SNPdbe | rs11075997 |
MSV3d | rs11075997 |
GWAS Ctlg | rs11075997 |
GMAF | 0.3751 |
Max Magnitude | 0 |
? | (C;C) (C;T) (T;T) | 28 |
---|---|---|
|
[PMID 23251365] Genetic Variants in the Fat and Obesity Associated (FTO) Gene and Risk of Alzheimer's Disease