rs10999409
From SNPedia
Orientation | plus |
Stabilized | plus |
Make rs10999409(C;C) |
Make rs10999409(C;T) |
Make rs10999409(T;T) |
Reference | GRCh38 38.1/142 |
Chromosome | 10 |
Position | 70572684 |
is a | snp |
is | mentioned by |
dbSNP | rs10999409 |
dbSNP (classic) | rs10999409 |
ClinGen | rs10999409 |
ebi | rs10999409 |
HLI | rs10999409 |
Exac | rs10999409 |
Gnomad | rs10999409 |
Varsome | rs10999409 |
LitVar | rs10999409 |
Map | rs10999409 |
PheGenI | rs10999409 |
Biobank | rs10999409 |
1000 genomes | rs10999409 |
hgdp | rs10999409 |
ensembl | rs10999409 |
geneview | rs10999409 |
scholar | rs10999409 |
rs10999409 | |
pharmgkb | rs10999409 |
gwascentral | rs10999409 |
openSNP | rs10999409 |
23andMe | rs10999409 |
SNPshot | rs10999409 |
SNPdbe | rs10999409 |
MSV3d | rs10999409 |
GWAS Ctlg | rs10999409 |
GMAF | 0.4793 |
Max Magnitude | 0 |
? | (C;C) (C;T) (T;T) | 28 |
---|---|---|
|
GWAS snp | |
---|---|
PMID | [PMID 19553259![]() |
Trait | Obesity (extreme) |
Title | Common BMI-associated variants confer risk of extreme obesity |
Risk Allele | T |
P-val | 0.000005 |
Odds Ratio | 1.30 [1.16-1.45] |