rs62048402
From SNPedia
Orientation | plus |
Stabilized | plus |
Make rs62048402(A;A) |
Make rs62048402(A;G) |
Make rs62048402(G;G) |
Reference | GRCh38 38.1/141 |
Chromosome | 16 |
Position | 53769311 |
Gene | FTO |
is a | snp |
is | mentioned by |
dbSNP | rs62048402 |
dbSNP (classic) | rs62048402 |
ClinGen | rs62048402 |
ebi | rs62048402 |
HLI | rs62048402 |
Exac | rs62048402 |
Gnomad | rs62048402 |
Varsome | rs62048402 |
LitVar | rs62048402 |
Map | rs62048402 |
PheGenI | rs62048402 |
Biobank | rs62048402 |
1000 genomes | rs62048402 |
hgdp | rs62048402 |
ensembl | rs62048402 |
geneview | rs62048402 |
scholar | rs62048402 |
rs62048402 | |
pharmgkb | rs62048402 |
gwascentral | rs62048402 |
openSNP | rs62048402 |
23andMe | rs62048402 |
SNPshot | rs62048402 |
SNPdbe | rs62048402 |
MSV3d | rs62048402 |
GWAS Ctlg | rs62048402 |
GMAF | 0.2479 |
Max Magnitude | 0 |
[PMID 23860325] Polymorphisms in FTO and near TMEM18 associate with type 2 diabetes and predispose to younger age at diagnosis of diabetes
[PMID 24385306] The role of common and rare MC4R variants and FTO polymorphisms in extreme form of obesity